HRP970663A2 - Parasiticidal pyrazoles - Google Patents
Parasiticidal pyrazolesInfo
- Publication number
- HRP970663A2 HRP970663A2 HR9712045.5A HRP970663A HRP970663A2 HR P970663 A2 HRP970663 A2 HR P970663A2 HR P970663 A HRP970663 A HR P970663A HR P970663 A2 HRP970663 A2 HR P970663A2
- Authority
- HR
- Croatia
- Prior art keywords
- dichloro
- cyano
- halo
- pyrazole
- hydrogen
- Prior art date
Links
- 150000003217 pyrazoles Chemical class 0.000 title description 3
- 230000000590 parasiticidal effect Effects 0.000 title 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 351
- 150000001875 compounds Chemical class 0.000 claims description 281
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 145
- 238000002360 preparation method Methods 0.000 claims description 138
- 239000000203 mixture Substances 0.000 claims description 97
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 77
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 77
- 239000001257 hydrogen Substances 0.000 claims description 61
- 229910052739 hydrogen Inorganic materials 0.000 claims description 61
- 125000005843 halogen group Chemical group 0.000 claims description 57
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 45
- 150000002431 hydrogen Chemical class 0.000 claims description 44
- 239000002904 solvent Substances 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 37
- DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 claims description 36
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical group [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 claims description 34
- 238000010992 reflux Methods 0.000 claims description 32
- 150000003839 salts Chemical class 0.000 claims description 31
- -1 2,4,6-trisubstituted phenyl Chemical group 0.000 claims description 30
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 23
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 23
- 125000001246 bromo group Chemical group Br* 0.000 claims description 22
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 20
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical group C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 claims description 20
- 238000009472 formulation Methods 0.000 claims description 20
- 239000012453 solvate Substances 0.000 claims description 20
- 241001465754 Metazoa Species 0.000 claims description 19
- 239000003054 catalyst Substances 0.000 claims description 19
- 238000006243 chemical reaction Methods 0.000 claims description 19
- 229950005228 bromoform Drugs 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- LXNAVEXFUKBNMK-UHFFFAOYSA-N palladium(II) acetate Substances [Pd].CC(O)=O.CC(O)=O LXNAVEXFUKBNMK-UHFFFAOYSA-N 0.000 claims description 14
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical group [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 claims description 14
- PLHSKXBFZPAQOD-UHFFFAOYSA-N phenyl(tribromomethyl)mercury Chemical compound BrC(Br)(Br)[Hg]C1=CC=CC=C1 PLHSKXBFZPAQOD-UHFFFAOYSA-N 0.000 claims description 11
- 229910052723 transition metal Inorganic materials 0.000 claims description 11
- 150000003624 transition metals Chemical class 0.000 claims description 11
- 238000011282 treatment Methods 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000001153 fluoro group Chemical group F* 0.000 claims description 10
- SOWFJRRENUZFJD-UHFFFAOYSA-N 4-(2,2-dibromocyclopropyl)-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]pyrazole-3-carbonitrile Chemical compound ClC1=CC(C(F)(F)F)=CC(Cl)=C1N1N=C(C#N)C(C2C(C2)(Br)Br)=C1 SOWFJRRENUZFJD-UHFFFAOYSA-N 0.000 claims description 9
- 239000002585 base Substances 0.000 claims description 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 9
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 7
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000003153 chemical reaction reagent Substances 0.000 claims description 7
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 7
- 238000001149 thermolysis Methods 0.000 claims description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
- 125000004775 chlorodifluoromethyl group Chemical group FC(F)(Cl)* 0.000 claims description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 230000003071 parasitic effect Effects 0.000 claims description 6
- 239000008096 xylene Substances 0.000 claims description 6
- DRBAAFANJKSJOI-UHFFFAOYSA-N 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[1-(trifluoromethyl)cyclopropyl]pyrazole-3-carbonitrile Chemical compound ClC1=CC(C(F)(F)F)=CC(Cl)=C1N1N=C(C#N)C(C2(CC2)C(F)(F)F)=C1 DRBAAFANJKSJOI-UHFFFAOYSA-N 0.000 claims description 5
- 230000002141 anti-parasite Effects 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 239000003814 drug Substances 0.000 claims description 5
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 5
- FMCJEPSLAMDJTN-UHFFFAOYSA-N 4-(2,2-dichlorocyclopropyl)-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]pyrazole-3-carbonitrile Chemical compound ClC1=CC(C(F)(F)F)=CC(Cl)=C1N1N=C(C#N)C(C2C(C2)(Cl)Cl)=C1 FMCJEPSLAMDJTN-UHFFFAOYSA-N 0.000 claims description 4
- JPCAVYRPGUDXAK-UHFFFAOYSA-N 4-[1-chloro-2-(difluoromethyl)cyclopropyl]-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]pyrazole-3-carbonitrile Chemical compound FC(F)C1CC1(Cl)C1=CN(C=2C(=CC(=CC=2Cl)C(F)(F)F)Cl)N=C1C#N JPCAVYRPGUDXAK-UHFFFAOYSA-N 0.000 claims description 4
- ZFHFCQOBLUMTCL-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[1-(trifluoromethyl)cyclopropyl]pyrazole-3-carbonitrile Chemical compound NC1=C(C2(CC2)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZFHFCQOBLUMTCL-UHFFFAOYSA-N 0.000 claims description 4
- VUGACNDBOVRKKT-UHFFFAOYSA-N 5-amino-4-(2,2-dibromocyclopropyl)-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]pyrazole-3-carbonitrile Chemical compound N#CC1=NN(C=2C(=CC(=CC=2Cl)C(F)(F)F)Cl)C(N)=C1C1CC1(Br)Br VUGACNDBOVRKKT-UHFFFAOYSA-N 0.000 claims description 4
- 239000003096 antiparasitic agent Substances 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 claims description 4
- 239000002689 soil Substances 0.000 claims description 4
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims description 3
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 3
- 125000001033 ether group Chemical group 0.000 claims description 3
- 125000006343 heptafluoro propyl group Chemical group 0.000 claims description 3
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 125000001624 naphthyl group Chemical group 0.000 claims description 3
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 3
- 239000012429 reaction media Substances 0.000 claims description 3
- 241000282412 Homo Species 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 2
- 229940125687 antiparasitic agent Drugs 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 238000003408 phase transfer catalysis Methods 0.000 claims description 2
- MVIAEGXPYBMVPT-UHFFFAOYSA-N phenyl(trichloromethyl)mercury Chemical compound ClC(Cl)(Cl)[Hg]C1=CC=CC=C1 MVIAEGXPYBMVPT-UHFFFAOYSA-N 0.000 claims description 2
- ITDJKCJYYAQMRO-UHFFFAOYSA-L rhodium(2+);diacetate Chemical group [Rh+2].CC([O-])=O.CC([O-])=O ITDJKCJYYAQMRO-UHFFFAOYSA-L 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 2
- 125000001589 carboacyl group Chemical group 0.000 claims 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 309
- 239000000243 solution Substances 0.000 description 151
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 113
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 108
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 97
- 239000003480 eluent Substances 0.000 description 87
- 239000007787 solid Substances 0.000 description 84
- 239000011541 reaction mixture Substances 0.000 description 81
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 75
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 72
- 239000000741 silica gel Substances 0.000 description 71
- 229910002027 silica gel Inorganic materials 0.000 description 71
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 69
- 238000004440 column chromatography Methods 0.000 description 64
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 42
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 36
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 32
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 28
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 25
- 238000002425 crystallisation Methods 0.000 description 23
- 230000008025 crystallization Effects 0.000 description 23
- 239000012074 organic phase Substances 0.000 description 23
- 239000012265 solid product Substances 0.000 description 23
- 239000012267 brine Substances 0.000 description 22
- 238000004007 reversed phase HPLC Methods 0.000 description 22
- 239000003921 oil Substances 0.000 description 21
- 235000019198 oils Nutrition 0.000 description 21
- 239000000377 silicon dioxide Substances 0.000 description 21
- 239000002244 precipitate Substances 0.000 description 19
- 239000007832 Na2SO4 Substances 0.000 description 17
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 17
- 239000011259 mixed solution Substances 0.000 description 17
- 229910052938 sodium sulfate Inorganic materials 0.000 description 17
- 235000011152 sodium sulphate Nutrition 0.000 description 17
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 16
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 16
- 235000019341 magnesium sulphate Nutrition 0.000 description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- LQZMLBORDGWNPD-UHFFFAOYSA-N N-iodosuccinimide Chemical compound IN1C(=O)CCC1=O LQZMLBORDGWNPD-UHFFFAOYSA-N 0.000 description 14
- 239000000284 extract Substances 0.000 description 14
- 229910052757 nitrogen Inorganic materials 0.000 description 14
- IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 14
- QIWRFOJWQSSRJZ-UHFFFAOYSA-N tributyl(ethenyl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C=C QIWRFOJWQSSRJZ-UHFFFAOYSA-N 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 13
- 241000238631 Hexapoda Species 0.000 description 12
- 239000008346 aqueous phase Substances 0.000 description 12
- 241000196324 Embryophyta Species 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 239000012043 crude product Substances 0.000 description 10
- 238000001704 evaporation Methods 0.000 description 10
- 241000238421 Arthropoda Species 0.000 description 9
- 241000255925 Diptera Species 0.000 description 9
- 241000258937 Hemiptera Species 0.000 description 9
- 238000010828 elution Methods 0.000 description 9
- 230000008020 evaporation Effects 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 235000013339 cereals Nutrition 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 7
- 150000001336 alkenes Chemical class 0.000 description 7
- 239000000543 intermediate Substances 0.000 description 7
- 238000000746 purification Methods 0.000 description 7
- 238000001665 trituration Methods 0.000 description 7
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 6
- AQRLNPVMDITEJU-UHFFFAOYSA-N triethylsilane Chemical compound CC[SiH](CC)CC AQRLNPVMDITEJU-UHFFFAOYSA-N 0.000 description 6
- 241000256602 Isoptera Species 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 238000004128 high performance liquid chromatography Methods 0.000 description 5
- 125000002346 iodo group Chemical group I* 0.000 description 5
- VUPQHSHTKBZVML-UHFFFAOYSA-J rhodium(3+);tetraacetate Chemical compound [Rh+3].[Rh+3].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O VUPQHSHTKBZVML-UHFFFAOYSA-J 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 239000012258 stirred mixture Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
- 241000238876 Acari Species 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 241000607479 Yersinia pestis Species 0.000 description 4
- LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 4
- 239000012230 colorless oil Substances 0.000 description 4
- 235000013399 edible fruits Nutrition 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 229910052740 iodine Inorganic materials 0.000 description 4
- 239000011630 iodine Substances 0.000 description 4
- VXWPONVCMVLXBW-UHFFFAOYSA-M magnesium;carbanide;iodide Chemical compound [CH3-].[Mg+2].[I-] VXWPONVCMVLXBW-UHFFFAOYSA-M 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- 238000010898 silica gel chromatography Methods 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 4
- 125000004961 1-arylpyrazolyl group Chemical group 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 241000219146 Gossypium Species 0.000 description 3
- 241000255967 Helicoverpa zea Species 0.000 description 3
- 241000257303 Hymenoptera Species 0.000 description 3
- 206010061217 Infestation Diseases 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
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- JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 1
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- 229940074928 isopropyl myristate Drugs 0.000 description 1
- 230000000155 isotopic effect Effects 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
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- 229940126601 medicinal product Drugs 0.000 description 1
- 229940101209 mercuric oxide Drugs 0.000 description 1
- 229910000474 mercury oxide Inorganic materials 0.000 description 1
- BQPIGGFYSBELGY-UHFFFAOYSA-N mercury(2+) Chemical class [Hg+2] BQPIGGFYSBELGY-UHFFFAOYSA-N 0.000 description 1
- JMKJCPUVEMZGEC-UHFFFAOYSA-N methyl 2,2,3,3,3-pentafluoropropanoate Chemical compound COC(=O)C(F)(F)C(F)(F)F JMKJCPUVEMZGEC-UHFFFAOYSA-N 0.000 description 1
- MRPUVAKBXDBGJQ-UHFFFAOYSA-N methyl 2,2,3,3,4,4,4-heptafluorobutanoate Chemical compound COC(=O)C(F)(F)C(F)(F)C(F)(F)F MRPUVAKBXDBGJQ-UHFFFAOYSA-N 0.000 description 1
- LSEFCHWGJNHZNT-UHFFFAOYSA-M methyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 LSEFCHWGJNHZNT-UHFFFAOYSA-M 0.000 description 1
- XSGHLZBESSREDT-UHFFFAOYSA-N methylenecyclopropane Chemical compound C=C1CC1 XSGHLZBESSREDT-UHFFFAOYSA-N 0.000 description 1
- QIRVGKYPAOQVNP-UHFFFAOYSA-N methylidenecyclobutane Chemical compound C=C1CCC1 QIRVGKYPAOQVNP-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- UAWYLGHYOSGLML-UHFFFAOYSA-N n-[[3-cyano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]pyrazol-4-yl]methylideneamino]-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NN=CC1=CN(C=2C(=CC(=CC=2Cl)C(F)(F)F)Cl)N=C1C#N UAWYLGHYOSGLML-UHFFFAOYSA-N 0.000 description 1
- IOMMMLWIABWRKL-WUTDNEBXSA-N nazartinib Chemical compound C1N(C(=O)/C=C/CN(C)C)CCCC[C@H]1N1C2=C(Cl)C=CC=C2N=C1NC(=O)C1=CC=NC(C)=C1 IOMMMLWIABWRKL-WUTDNEBXSA-N 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- PIDFDZJZLOTZTM-KHVQSSSXSA-N ombitasvir Chemical compound COC(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)NC1=CC=C([C@H]2N([C@@H](CC2)C=2C=CC(NC(=O)[C@H]3N(CCC3)C(=O)[C@@H](NC(=O)OC)C(C)C)=CC=2)C=2C=CC(=CC=2)C(C)(C)C)C=C1 PIDFDZJZLOTZTM-KHVQSSSXSA-N 0.000 description 1
- 229940126701 oral medication Drugs 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- MUJIDPITZJWBSW-UHFFFAOYSA-N palladium(2+) Chemical compound [Pd+2] MUJIDPITZJWBSW-UHFFFAOYSA-N 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- YNWSXIWHOSSPCO-UHFFFAOYSA-N rhodium(2+) Chemical group [Rh+2] YNWSXIWHOSSPCO-UHFFFAOYSA-N 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 210000003491 skin Anatomy 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- HHBXWXJLQYJJBW-UHFFFAOYSA-M triphenyl(propan-2-yl)phosphanium;iodide Chemical compound [I-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C(C)C)C1=CC=CC=C1 HHBXWXJLQYJJBW-UHFFFAOYSA-M 0.000 description 1
- 239000013598 vector Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/16—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pyridine Compounds (AREA)
Description
Ovaj izum se odnosi na derivate pirazola koji imaju antiparazitske osobine. Preciznije, on se odnosi na 1-aril-4-ciklopropilpirazole. This invention relates to pyrazole derivatives having antiparasitic properties. More precisely, it refers to 1-aryl-4-cyclopropylpyrazoles.
Neki derivati pirazola koji imaju, inter alia, antiparazitsku aktivnost veÄ su poznati. Na primjer, EP-A-0234119 opisuje 1-arilpirazole za kontrolu artropoda, sadnice nematoda i napasti crijevne gliste. 1-arilpirazoli su takoÄer opisani i u EP-A-0295117; dalje kako imaju artropodikidalnu, nematokidalnog nasada i antelminitsku aktivnost, ovi navedeni spojevi pokazuju antiprotozalne osobine. SliÄni profili aktivnosti takoÄer su prikazani u 1-arilpirazolima opisanim u EP-A-0295118. Some pyrazole derivatives having, inter alia, antiparasitic activity are already known. For example, EP-A-0234119 describes 1-arylpyrazoles for the control of arthropods, seedling nematodes and roundworm infestations. 1-Arylpyrazoles are also described in EP-A-0295117; further, as they have arthropodicidal, nematocidal plant and anthelmintic activity, these mentioned compounds show antiprotozoal properties. Similar activity profiles are also shown in the 1-arylpyrazoles described in EP-A-0295118.
Ovaj izum predviÄa spoj formule (I): This invention provides a compound of formula (I):
[image] [image]
ili njegovu farmaceutski, veterinarski ili agrokulturalno prihvatljivu sol, ili farmaceutski, veterinarski ili agrokulturalno prihvatljiv solvat (ukljuÄujuÄi hidrat) bilo kojeg entiteta, or its pharmaceutical, veterinary or agroculturally acceptable salt, or its pharmaceutical, veterinary or agroculturally acceptable solvate (including hydrate) of any entity,
gdje where
R1 je 2,4,6-trisupstituirani fenil gdje su 2- i 6-supstituenti svaki neovisno odabrani od halo-a i 4-supstituent je odabran od C1 do C4 alkila opcionalno supstituiranog sa jednim ili viŔe halo-a, C1 do C4 alkoksi opcionalno je supstituiranog sa jednim ili viŔe halo-a, S(O)nC1 do C4 alkila opcionalno supstituiranog sa jednim ili viŔe halo-a, halo i pentafluorotio, ili 3,5-disupstituirani piridin-2-il, gdje je 3-supstituent halo i 5-supstituent odabran od C1 do C4 alkila opcionalno supstituiranog sa jednim ili viŔe halo-a, C1 do C4 alkoksi opcionalno supstituiranog sa jednim ili viŔe halo-a, S(O)nC1 do C4 alkila opcionalno supstituiranog sa jednim ili viŔe halo-a, halo i pentafluorotio; R1 is 2,4,6-trisubstituted phenyl wherein the 2- and 6-substituents are each independently selected from halo and the 4-substituent is selected from C1 to C4 alkyl optionally substituted with one or more halo, C1 to C4 alkoxy is optionally substituted with one or more halo, S(O)nC1 to C4 alkyl optionally substituted with one or more halo, halo and pentafluorothio, or 3,5-disubstituted pyridin-2-yl, where the 3-substituent is halo and a 5-substituent selected from C1 to C4 alkyl optionally substituted with one or more halo, C1 to C4 alkoxy optionally substituted with one or more halo, S(O)nC1 to C4 alkyl optionally substituted with one or more halo -a, halo and pentafluorothio;
R3 je C1 do C4 alkil opcionalno supstituiran sa hidroksi ili sa jednim ili viŔe halo-a, cijano, C1 do C5 alkanoil ili fenil; R 3 is C 1 to C 4 alkyl optionally substituted with hydroxy or with one or more halo, cyano, C 1 to C 5 alkanoyl or phenyl;
R5 je vodik, C1 do C4 alkil, amino ili halo; R 5 is hydrogen, C 1 to C 4 alkyl, amino or halo;
R2 i R4 su svaki neovisno odabrani od vodika, C1 do C4 alkila, fluoro, kloro i bromo ili, zajedno sa atomom ugljika na koji su vezani, formiraju C3 do C6 cikloalkil grupu; R 2 and R 4 are each independently selected from hydrogen, C 1 to C 4 alkyl, fluoro, chloro and bromo or, together with the carbon atom to which they are attached, form a C 3 to C 6 cycloalkyl group;
R6 i R8 su svaki neovisno odabrani od vodika, C1 do C4 alkila, fluoro, kloro i bromo; R 6 and R 8 are each independently selected from hydrogen, C 1 to C 4 alkyl, fluoro, chloro and bromo;
ili, kada R2 i R4 ne formiraju dio cikloalkilne grupe, R2 i R6, zajedno sa atomima ugljika na koje su vezani, mogu formirati C5 do C7 cikloalkil grupu; or, when R 2 and R 4 do not form part of a cycloalkyl group, R 2 and R 6 , together with the carbon atoms to which they are attached, may form a C 5 to C 7 cycloalkyl group;
R7 je vodik, C1 do C4 alkil opcionalno supstituiran sa jednim ili viŔe halo-a, ili C1 do C4 alkoksi; i R 7 is hydrogen, C 1 to C 4 alkyl optionally substituted with one or more halo, or C 1 to C 4 alkoxy; and
n je 0, 1 ili 2. n is 0, 1 or 2.
U gornjoj definiciji, ako nije drugaÄije naznaÄeno, alkil i alkoksi grupe koje imaju 3 ili viÅ”e atoma ugljika i alkanoil grupe koje imaju 4 ili viÅ”e atoma ugljika mogu imati normalni ili raÄvasti lanac; halo oznaÄava fluoro, kloro, bromo ili jodo. In the above definition, unless otherwise indicated, alkyl and alkoxy groups having 3 or more carbon atoms and alkanoyl groups having 4 or more carbon atoms may be straight or branched chain; halo means fluoro, chloro, bromo or iodo.
Spojevi formule (I) mogu sadržavati jedan ili viÅ”e hiralnih centara i zato mogu postojati kao stereoizomeri, tj. kao enantiomeri ili diastereoizomeri, isto kao i njihove smjese. Izum ukljuÄuje oba pojedinaÄna stereoizomera spojeva formule (I) zajedno sa njihovim smjesama. Izdvajanje diastereoizomera može se postiÄi konvencionalnim tehnikama, napr. sa frakcijskom kristalizacijom kromatografije (ukljuÄujuÄi HPLC) diastereoizomerne smjese spoja formule (I) ili prikladne soli ili njenog derivata. PojedinaÄni enantiomer spoja formule (I) može se dobiti iz odgovarajuÄeg optiÄki Äistog intermedijera ili otapanjem, ili sa HPLC racemata koristeÄi prikladni hiralni nosaÄ ili, gdje je to prikladno, frakcijskom kristalizacijom diastereoizomernih soli formiranih reakcijom racemata sa prikladnom optiÄki aktivnom kiselinom. The compounds of formula (I) may contain one or more chiral centers and therefore may exist as stereoisomers, i.e. as enantiomers or diastereoisomers, as well as their mixtures. The invention includes both individual stereoisomers of compounds of formula (I) together with mixtures thereof. Separation of diastereoisomers can be achieved by conventional techniques, e.g. with fractional crystallization by chromatography (including HPLC) of a diastereoisomeric mixture of a compound of formula (I) or a suitable salt or derivative thereof. A single enantiomer of a compound of formula (I) can be obtained from the appropriate optically pure intermediate either by dissolution, or from the HPLC racemate using a suitable chiral support or, where appropriate, by fractional crystallization of the diastereoisomeric salts formed by reaction of the racemate with a suitable optically active acid.
U izum su takoÄer ukljuÄeni i radioaktivni derivati spojeva formule (I) koji su prikladni za bioloÅ”ke studije. Also included in the invention are radioactive derivatives of compounds of formula (I) which are suitable for biological studies.
Farmaceutski, veterinarski ili agrokulturalno prihvatljive soli spojeva formule (I) su, na primjer, netoksiÄne adicijske soli kiseline formirane sa neorganskim kiselinama takvim kao Å”to su klorovodikova kiselina, bromovodikova kiselina, sumporna i fosforna kiselina, sa organo-karboksilnim kiselinama, ili sa organo-sulfonskim kiselinama. Za pregled prikladnih soli, pogledati "J. Pharm. Sci.", 66, 1, (1977.). Pharmaceutically, veterinary or agroculturally acceptable salts of compounds of formula (I) are, for example, non-toxic acid addition salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric and phosphoric acid, with organo-carboxylic acids, or with organo- sulfonic acids. For a review of suitable salts, see "J. Pharm. Sci.", 66, 1, (1977).
Poželjna grupa spojeva formule (I) je ona gdje R1 je 2,6-dikloro-4-trifluorometilfenil, 2,6-dikloro-4-pentafluorotiofenil, 2,4,6-triklorofenil ili 3-kloro-5-trifluorometilpiridin-2-il; R3 je metil, etil, prop-2-il, 1-hidroksietil, 2-hidroksiprop-2-il, difluorometil, diklorometil, trifluorometil, cijano, formil, acetil ili fenil; R5 je vodik, metil, amino ili kloro; R2 i R4 su svaki neovisno odabrani od vodika, metila, fluoro, kloro i bromo ili, zajedno sa atomom ugljika na koji su vezani, formiraju ciklopropil, ciklobutil ili ciklopentil grupu; R6 i R8 su svaki neovisno odabrani od vodika, metila, kloro i bromo; ili, kada R2 i R4 ne formiraju dio cikloalkil grupe, R2 i R6, zajedno sa atomima ugljika na koje su vezani, mogu formirati ciklopentan ili cikloheksan grupu; i R7 je vodik, metil, etil, trifluorometil, klorodifluorometil, pentafluoroetil, heptafluoropropil ili metoksi. A preferred group of compounds of formula (I) is that where R 1 is 2,6-dichloro-4-trifluoromethylphenyl, 2,6-dichloro-4-pentafluorothiophenyl, 2,4,6-trichlorophenyl or 3-chloro-5-trifluoromethylpyridine-2- or R 3 is methyl, ethyl, prop-2-yl, 1-hydroxyethyl, 2-hydroxyprop-2-yl, difluoromethyl, dichloromethyl, trifluoromethyl, cyano, formyl, acetyl or phenyl; R 5 is hydrogen, methyl, amino or chloro; R 2 and R 4 are each independently selected from hydrogen, methyl, fluoro, chloro and bromo or, together with the carbon atom to which they are attached, form a cyclopropyl, cyclobutyl or cyclopentyl group; R 6 and R 8 are each independently selected from hydrogen, methyl, chloro and bromo; or, when R 2 and R 4 do not form part of a cycloalkyl group, R 2 and R 6 , together with the carbon atoms to which they are attached, may form a cyclopentane or cyclohexane group; and R 7 is hydrogen, methyl, ethyl, trifluoromethyl, chlorodifluoromethyl, pentafluoroethyl, heptafluoropropyl or methoxy.
Poželjnija grupa spojeva formule (I) je ona gdje R1 je 2,6-dikloro-4-trifluorometilfenil, 2,6-dikloro-4-pentafluorotiofenil ili 3-kloro-5-trifluorometilpiridin-2-il; R3 je cijano; R5 je vodik ili amino; R2 i R4 su isti i oni su vodik, kloro ili bromo; R6 i R8 su vodik; i R7 je vodik, trifluorometil ili klorodifluorometil. A more preferred group of compounds of formula (I) is one where R 1 is 2,6-dichloro-4-trifluoromethylphenyl, 2,6-dichloro-4-pentafluorothiophenyl or 3-chloro-5-trifluoromethylpyridin-2-yl; R 3 is cyano; R 5 is hydrogen or amino; R 2 and R 4 are the same and are hydrogen, chloro or bromo; R 6 and R 8 are hydrogen; and R 7 is hydrogen, trifluoromethyl or chlorodifluoromethyl.
Posebno poželjni pojedinaÄni spojevi iz izuma ukljuÄuju: Particularly preferred individual compounds of the invention include:
3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol; 3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole;
(-)-3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol; (-)-3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole;
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(1-trifluorometilciklopropil)pirazol; 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-trifluoromethylcyclopropyl)pyrazole;
3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-pentafluorotiofenil)pirazol; 3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole;
3-ciano-4-(2,2-diklorociklopropil)-1-(2,6-dikloro-4-pentafluorotiofenil)pirazol; 3-cyano-4-(2,2-dichlorocyclopropyl)-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole;
3-ciano-4-(2,2-diklorociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol; 3-cyano-4-(2,2-dichlorocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole;
4-(1-klorodifluorometilciklopropil)-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol; 4-(1-chlorodifluoromethylcyclopropyl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole;
1-[(3-kloro-5-trifluorometil)piridin-2-il)]-3-ciano-4-(2,2-dibromociklopropil)pirazol; 1-[(3-chloro-5-trifluoromethyl)pyridin-2-yl)]-3-cyano-4-(2,2-dibromocyclopropyl)pyrazole;
5-amino-3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol; 5-amino-3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole;
5-amino-3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-pentafluorotiofenil)pirazol; 5-amino-3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole;
5-amino-3-ciano-4-(2,2-diklorociklopropil)-1-(2,6-dikloro-4-pentafluorotiofenil)pirazol; i 5-amino-3-cyano-4-(2,2-dichlorocyclopropyl)-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole; and
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(1-trifluorometilciklopropil)pirazol. 5-Amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-trifluoromethylcyclopropyl)pyrazole.
U daljnjem glediÅ”tu, ovaj izum osigurava postupke za dobivanje spoja formule (I), ili farmaceutski, veterinarski ili agrokulturalno prihvatljive njegove soli, ili farmaceutski, veterinarski ili agrokulturalno prihvatljivog solvata (ukljuÄujuÄi hidrat) bilo kojeg entiteta, kako je niže ilustrirano. StruÄnjaci Äe primijetiti da, unutar nekih opisanih postupaka, red koriÅ”tenih sintetiÄkih faza se može mijenjati i ovisiti Äe inter alia od faktora kao Å”to su priroda drugih funkcionalnih grupa prisutnih u odreÄenom supstratu, raspoloživosti kljuÄnih intermedijera, i strategije zaÅ”titne grupe koju treba izabrati. Jasno, takvi faktori Äe takoÄer utjecati na izbor reagensa za primjenu u spomenutim sintetiÄkim fazama. Treba se takoÄer primijetiti da Äe razne meÄukonverzije i transformacije standardnog supstituenta ili funkcionalne grupe unutar nekih spojeva formule (I) osigurati druge spojeve formule (I). Primjeri su deaminacija spoja formule (I) gdje je R5 amino, monodebrominacija spoja formule (I) gdje su R2 i R4 bromo, i konverzije spoja formule (I) gdje je R3 ciano, spoj formule (I) gdje R3 je C1 do C5 alkanoil, spoj formule (I) gdje R3 je C1 do C4 alkanoil spoju formule (I) gdje R3 je C1 do C4 alkil supstituiran sa hidroksi ili sa dihalo, i spoj formule (I) gdje R3 alkil je supstituiran sa hidroksi spoju formule (I) gdje R3 je C1 do C4 alkil ili C1 do C4 alkil monosupstituiran sa halo. In a further aspect, the present invention provides processes for preparing a compound of formula (I), or a pharmaceutically, veterinary or agroculturally acceptable salt thereof, or a pharmaceutically, veterinary or agroculturally acceptable solvate (including a hydrate) of any entity, as illustrated below. Those skilled in the art will note that, within some of the procedures described, the order of synthetic steps used may vary and will depend inter alia on factors such as the nature of other functional groups present in a particular substrate, the availability of key intermediates, and the protecting group strategy to be chosen. Clearly, such factors will also influence the choice of reagents for use in the mentioned synthetic phases. It should also be noted that various interconversions and transformations of a standard substituent or functional group within some compounds of formula (I) will provide other compounds of formula (I). Examples are deamination of a compound of formula (I) where R5 is amino, monodebromination of a compound of formula (I) where R2 and R4 are bromo, and conversions of a compound of formula (I) where R3 is cyano, a compound of formula (I) where R3 is C1 to C5 alkanoyl , the compound of formula (I) where R3 is C1 to C4 alkanoyl to the compound of formula (I) where R3 is C1 to C4 alkyl substituted with hydroxy or dihalo, and the compound of formula (I) where R3 is alkyl substituted with hydroxy to the compound of formula (I) where R 3 is C 1 to C 4 alkyl or C 1 to C 4 alkyl monosubstituted with halo.
Tako su slijedeÄi postupci ilustrativni za opÄe sintetiÄke postupke koji se mogu izabrati za dobivanje spojeva iz izuma. Thus, the following procedures are illustrative of the general synthetic procedures that may be chosen to obtain the compounds of the invention.
1. Spoj formule (I) se može dobiti ciklopropanacijom alkena formule (II): 1. The compound of formula (I) can be obtained by cyclopropanation of alkene of formula (II):
[image] [image]
gdje su R1, R3, R5, R6, R7 i R8 kako je prije definirano za formulu (I). Ovo se može postiÄi in situ stvaranjem zahtjevanih karbenoid vrsta, u prisustvu spoja formule (II), prikladnom metodom. Takve metode ukljuÄuju tretman kloroforma ili bromoforma sa bazom, poželjno pod uvjetima katalize prijenosa faze, termolize prikladnog organometalnog prethodnika takvog kao aril triklorometil ili tribromometil derivat žive, tretmana sa diazoalkanom u prisustvu katalizatora tranzicijskog metala i tretmana sa diazoalkanom u odsustvu katalizatora tranzicijskog metala praÄeno sa termolizom intermedijera pirazolina. where R 1 , R 3 , R 5 , R 6 , R 7 and R 8 are as previously defined for formula (I). This can be achieved by in situ formation of the required carbenoid species, in the presence of a compound of formula (II), by a suitable method. Such methods include treatment of chloroform or bromoform with a base, preferably under conditions of phase transfer catalysis, thermolysis of a suitable organometallic precursor such as an aryl trichloromethyl or tribromomethyl derivative of mercury, treatment with a diazoalkane in the presence of a transition metal catalyst, and treatment with a diazoalkane in the absence of a transition metal catalyst followed by thermolysis of the pyrazoline intermediate.
Na primjer u prvoj metodi, za dobivanje spoja formule (I) gdje su R2 i R4 ili oba kloro ili oba bromo, kloroform ili bromoform se tretira sa koncentriranom vodenom otopinom hidroksida alkalnog metala u prisustvu spoja formule (II) i kvaternarne amonijeve soli u prikladnom otapalu na temperaturi od oko sobne do oko temperature refluksa reakcijske sredine. Poželjni reagensi su natrij hidroksid i benziltrietilamonij klorid respektivno, dok je otapalo poželjno diklorometan opcionalno u prisustvu male koliÄine etanola. For example in the first method, to obtain a compound of formula (I) where R 2 and R 4 are either both chloro or both bromo, chloroform or bromoform is treated with a concentrated aqueous alkali metal hydroxide solution in the presence of a compound of formula (II) and a quaternary ammonium salt in a suitable solvent at a temperature from about room temperature to about the reflux temperature of the reaction medium. The preferred reagents are sodium hydroxide and benzyltriethylammonium chloride respectively, while the solvent is preferably dichloromethane optionally in the presence of a small amount of ethanol.
U drugoj metodi na primjer, za dobivanje spoja formule (I) gdje su i R2 i R4 ili oba kloro ili oba bromo, smjesa spoja formule (II) i ili feniltriklorometilživa ili feniltribromometilživa respektivno se grije na od oko 60Ā°C do oko 75Ā°C u prikladnom otapalu, poželjno toluenu, ksilenu ili njihovoj smjesi. In another method, for example, to obtain a compound of formula (I) where both R 2 and R 4 are either both chloro or both bromo, a mixture of a compound of formula (II) and either phenyltrichloromethylmercury or phenyltribromomethylmercury, respectively, is heated to from about 60Ā°C to about 75Ā° C in a suitable solvent, preferably toluene, xylene or their mixture.
TreÄa metoda je tipizirana tretmanom spoja formule (II) sa eterskom otopinom diazometana u prisustvu paladij (II) acetata na temperaturi od oko sobne u prikladnom otapalu, poželjno eteru, koji osigurava spoj formule (I) gdje su oba i R2 i R4 vodik. A third method is typified by treating the compound of formula (II) with an ethereal solution of diazomethane in the presence of palladium (II) acetate at room temperature in a suitable solvent, preferably ether, which provides a compound of formula (I) where both R2 and R4 are hydrogen.
Alternativna varijanta za dobivanje spoja formule (I) gdje su R2 i R4 vodik je preko pirazolin intermedijera formiranog koriÅ”tenjem prethodne metode u odsustvu paladij (II) acetata. SlijedeÄa termoliza izoliranog pirazolina u prikladnom otapalu, poželjno ksilenu na od oko 135Ā°C do oko 145Ā°C, daje zahtijevani spoj. An alternative variant for obtaining the compound of formula (I) where R 2 and R 4 are hydrogen is via the pyrazoline intermediate formed using the previous method in the absence of palladium (II) acetate. Subsequent thermolysis of the isolated pyrazoline in a suitable solvent, preferably xylene at from about 135Ā°C to about 145Ā°C, affords the desired compound.
Spoj formule (II) može se dobiti iz spoja formule (III): The compound of formula (II) can be obtained from the compound of formula (III):
[image] [image]
gdje X je bromo ili jodo, i R1, R3 i R5 su kako je prije definirano za formulu (II), pod uvjetom da R5 nije bromo ili jodo. Poželjno je X jodo. Transformacija se može postiÄi sa ukrÅ”tenom reakcijom spoja formule (III) kataliziranog-tranzicijskog metala sa prikladnim reagensom vinilacije u prikladnom, opcionalno depliniranom, otapalu. Poželjno tranzicijski metal je paladij a reagens vinilacije je derivat organotina. Na primjer, spoj formule (III) se tretira sa tri-n-butil(vinil)kositrom u prisustvu tetrakis(trifenilfosfin)paladija(0) u dimetilformamidu na temperaturi od oko sobne do oko 80Ā°C, radi dobivanja spoja formule (II) gdje su R7, R6 i R8 vodik. wherein X is bromo or iodo, and R 1 , R 3 and R 5 are as previously defined for formula (II), provided that R 5 is not bromo or iodo. X iodine is preferred. The transformation can be achieved by cross-reacting a catalyzed transition metal compound of formula (III) with a suitable vinylation reagent in a suitable, optionally depleted, solvent. Preferably, the transition metal is palladium and the vinylation reagent is an organotin derivative. For example, a compound of formula (III) is treated with tri-n-butyl(vinyl)tin in the presence of tetrakis(triphenylphosphine)palladium(0) in dimethylformamide at a temperature of about room temperature to about 80Ā°C, to obtain a compound of formula (II) where R7, R6 and R8 are hydrogen.
Alternativno, spoj formule (II) gdje je R5 vodik, C1 do C4 alkil ili halo može se dobiti koriŔtenjem konvencionalne Wittig tehnologije reagiranjem spoja formule (V): Alternatively, a compound of formula (II) where R 5 is hydrogen, C 1 to C 4 alkyl or halo can be prepared using conventional Wittig technology by reacting a compound of formula (V):
[image] [image]
gdje je R7 vodik ili C1 do C4 alkil opcionalno supstituiran sa jednim ili viŔe halo, R5 je vodik, C1 do C4 alkil ili halo, i R1 i R3 su kako je prije definirano za formulu (II), sa prikladnom alkilfosfonij soli-izvedenog fosforastog ilida. wherein R 7 is hydrogen or C 1 to C 4 alkyl optionally substituted with one or more halo, R 5 is hydrogen, C 1 to C 4 alkyl or halo, and R 1 and R 3 are as previously defined for formula (II), with a suitable alkylphosphonium salt-derived phosphorus ylide.
Na primjer tretman metiltrifenilfosfonij halida sa jakom bazom u prikladnom otapalu, praÄeno dodavanjem spoja formule (V), proizvesti Äe spoj formule (II) gdje su oba i R6 i R8 vodik. Poželjno bazni reagens je otopina n-butilltija u heksanu, otapalo je eter ili tetrahidrofuran i reakcija se vrÅ”i na temperaturi od oko sobne do oko 35Ā°C. For example, treatment of methyltriphenylphosphonium halide with a strong base in a suitable solvent, followed by addition of a compound of formula (V), will produce a compound of formula (II) wherein both R 6 and R 8 are hydrogen. Preferably, the basic reagent is a solution of n-butyllithium in hexane, the solvent is ether or tetrahydrofuran, and the reaction is carried out at a temperature from about room to about 35Ā°C.
Za spoj formule (II) gdje R7 je C1 do C4 alkoksi, R6 i R8 su vodik, R5 je vodik, C1 do C4 alkil ili halo, i R1 i R3 su kako je prije definirano za formulu (II), naroÄito je prikladno primjeniti niz meÄukonverzije alkena i time spoj formule (II), gdje su R7, R6 i R8 vodik, R5 je vodik, C1 do C4 alkil ili halo, i R1 i R3 su kako je prije definirano za formulu (II), tretira se sa jodom u prikladnom C1 do C4 alkanolu u prisustvu soli žive(II) radi osiguravanja intermedijera Ī±-alkoksi-Ī²(-jodoetilpirazola koji se, dalje, dehidrojodira sa prikladnom bazom, opcionalno u prikladnom otapalu. Na primjer, kada je R7 metoksi, prva faza se vrÅ”i koriÅ”tenjem živinog oksida i joda u metanolu na temperaturi oko refluksne temperature reakcijske sredine, dok se druga faza može vrÅ”iti koriÅ”tenjem baze tercijarnog amina takve kao 1,8-diazabiciklo[5,4,0]undek-7-en (DBU) u toluenu na sobnoj temperaturi. For a compound of formula (II) where R 7 is C 1 to C 4 alkoxy, R 6 and R 8 are hydrogen, R 5 is hydrogen, C 1 to C 4 alkyl or halo, and R 1 and R 3 are as previously defined for formula (II), it is particularly suitable to use a series of alkene interconversions and thus a compound of formula (II), where R7, R6 and R8 are hydrogen, R5 is hydrogen, C1 to C4 alkyl or halo, and R1 and R3 are as previously defined for formula (II), is treated with iodine in a suitable C1 to C4 alkanol in the presence of a mercury(II) salt to provide the intermediate Ī±-Alkoxy-Ī²(-iodoethylpyrazole which is further dehydroiodinated with a suitable base, optionally in a suitable solvent. For example, when R7 is methoxy, the first step is performed using mercury oxide and iodine in methanol at a temperature around the reflux temperature of the reaction medium, while the second stage can be performed using a tertiary amine base such as 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU) in toluene at room temperature.
Spoj formule (III) gdje je R5 vodik ili halo može se dobiti iz spoja formule (III) gdje je R5 amino sa konvencionalnim postupcima deaminacije ili deaminacije-halogenacije, respektivno. Kada je R5 vodik, prikladni postupak ukljuÄuje tretman amina sa t-butil nitritom u tetrahidrofuranu kao otapalu na temperaturi oko sobne do oko 70Ā°C. Kada je R5 , na primjer, kloro, otopina amina u prikladnom otapalu takvom kao acetonitril može se tretirati sa otopinom nitrosil klorida u diklorometanu na oko 0Ā°C praÄeno zagrijavanjem na temperaturi refuksa reakcijske smjese. A compound of formula (III) wherein R 5 is hydrogen or halo can be obtained from a compound of formula (III) wherein R 5 is amino by conventional deamination or deamination-halogenation procedures, respectively. When R5 is hydrogen, a convenient procedure involves treating the amine with t-butyl nitrite in tetrahydrofuran as a solvent at about room temperature to about 70Ā°C. When R5 is, for example, chloro, a solution of the amine in a suitable solvent such as acetonitrile can be treated with a solution of nitrosyl chloride in dichloromethane at about 0Ā°C followed by heating to the reflux temperature of the reaction mixture.
Na analogni naÄin, spoj formule (V) gdje je R5 vodik ili halo može se dobiti iz spoja formule (V) gdje je R5 amino. Ono posljednje, dalje, može se dobiti iz spoja formule (IV), gdje je R5 amino i R1 i R3 su kako je prethodno definirano za formulu (III), konvencionalnom acilacijom. In an analogous manner, a compound of formula (V) wherein R 5 is hydrogen or halo can be obtained from a compound of formula (V) wherein R 5 is amino. The latter, further, can be obtained from the compound of formula (IV), where R 5 is amino and R 1 and R 3 are as previously defined for formula (III), by conventional acylation.
Spoj formule (III) gdje R5 je C1 do C4 alkil ili amino takoÄer se može dobiti iz spoja formule (IV): The compound of formula (III) where R5 is C1 to C4 alkyl or amino can also be obtained from the compound of formula (IV):
[image] [image]
gdje R5 je C1 do C4 alkil ili amino i R1 i R3 su kako je ranije definirano za formulu (III), konvencionalnim postupcima brominacije ili jodinacije. Na primjer, kada je X jodo, spoj formule (IV) tretira se sa N-jodosukcinimidom u prikladnom otapalu takvom kao acetonitril na temperaturi oko sobne do oko 85Ā°C. wherein R 5 is C 1 to C 4 alkyl or amino and R 1 and R 3 are as previously defined for formula (III), by conventional bromination or iodination procedures. For example, when X is iodo, the compound of formula (IV) is treated with N-iodosuccinimide in a suitable solvent such as acetonitrile at about room temperature to about 85Ā°C.
Spoj formule (V) gdje je R7 vodik može se konvencionalno dobiti iz spoja formule (II) gdje su R7, R6 i R8 vodik, R5 je vodik, C1 do C4 alkil ili halo, i R1 i R3 su kako je prije definirano za formulu (II), oksidacijom vinil grupe bilo kojom varijantom standardnih postupaka. Na primjer, jedan takav postupak ukljuÄuje tretman alkena sa osmij tetroksidom u prisustvu 4-metilmorfolin-N-oksida u prikladnom otapalu, zatim slijedeÄi tretman reakcijske smjese sa natrij metaperiodatom. Poželjno osmij tetroksid se uvodi kao t-butanol otopina, reakcijsko otapalo je 90 % vodeni aceton i reakcija se vrÅ”i na temperaturi oko sobne. A compound of formula (V) wherein R 7 is hydrogen may be conventionally prepared from a compound of formula (II) wherein R 7 , R 6 and R 8 are hydrogen, R 5 is hydrogen, C 1 to C 4 alkyl or halo, and R 1 and R 3 are as previously defined for the formula (II), by oxidation of the vinyl group by any variant of standard procedures. For example, one such procedure involves treating the alkene with osmium tetroxide in the presence of 4-methylmorpholine-N-oxide in a suitable solvent, followed by treatment of the reaction mixture with sodium metaperiodate. Osmium tetroxide is preferably introduced as a t-butanol solution, the reaction solvent is 90% aqueous acetone and the reaction is carried out at room temperature.
Jasno, po analogiji, ovaj oksidacijski pristup može se takoÄer koristiti za dobivanje spoja formule (V) gdje R7 je C1 do C4 alkil opcionalno supstituiran sa jednim ili viÅ”e halo iz odgovarajuÄeg alkena. MeÄutim, kada je R7 metil, alternativni put ka spoju formule (V) je preko hidracije spoja formule (VI): Clearly, by analogy, this oxidation approach can also be used to prepare a compound of formula (V) wherein R 7 is C 1 to C 4 alkyl optionally substituted with one or more halos from the corresponding alkene. However, when R7 is methyl, an alternative route to a compound of formula (V) is via hydration of a compound of formula (VI):
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gdje je R8 vodik, i R1, R3 i R5 su kako je prije definirano za formulu (V). Prikladno, ovaj postupak može se takoÄer koristiti kada je R5 amino. where R 8 is hydrogen, and R 1 , R 3 and R 5 are as previously defined for formula (V). Conveniently, this procedure can also be used when R5 is amino.
Ovaj tretman alkina formule (VI) sa kiselinom u prikladnom otapalu na temperaturi oko sobne daje odgovarajuÄi derivat 4-acetilpirazola. Poželjno, kiselina je p-toluensulfonska kiselina i otapalo je acetonitril. This treatment of an alkyne of formula (VI) with an acid in a suitable solvent at room temperature gives the corresponding 4-acetylpyrazole derivative. Preferably, the acid is p-toluenesulfonic acid and the solvent is acetonitrile.
Dalje, spoj formule (VI) može se dobiti iz prikladnog zaÅ”tiÄenog prethodnika, npr. spoja formule (VI) gdje je R8 trimetilsilil. U takvom sluÄaju, skidanje zaÅ”tite može se vrÅ”iti koriÅ”tenjem blage baze takve kao kalij karbonat u prikladnom otapalu takvom kao metanol. Further, a compound of formula (VI) may be obtained from a suitable protected precursor, eg a compound of formula (VI) wherein R 8 is trimethylsilyl. In such a case, deprotection can be done using a mild base such as potassium carbonate in a suitable solvent such as methanol.
Prikladno, kada R5 nije bromo ili jodo, zaÅ”tiÄeni alkin je dostupan iz spoja formule (III) reakcijom ukrÅ”tenog spajanja kataliziranog-tranzicijskog metala sa trimetilsililacetilenom u prisustvu viÅ”ka tercijarne baze u prikladnom otapalu. Poželjno, tranzicijski metal je paladij. Tako, na primjer, spoj formule (III) se tretira sa trimetilsililacetilenom u prisustvu bis(trifenilfosfin)-paladij(II) klorida, bakar jodida i trietilamina u dimetilformamidu na od oko 45Ā°C do oko 65Ā°C. Conveniently, when R 5 is not bromo or iodo, the protected alkyne is available from a compound of formula (III) by a catalyzed transition-metal cross-coupling reaction with trimethylsilylacetylene in the presence of an excess of a tertiary base in a suitable solvent. Preferably, the transition metal is palladium. Thus, for example, a compound of formula (III) is treated with trimethylsilylacetylene in the presence of bis(triphenylphosphine)-palladium(II) chloride, copper iodide and triethylamine in dimethylformamide at from about 45Ā°C to about 65Ā°C.
2. Spoj formule (I) može se takoÄer dobiti strategijom alternativne ciklopropanacije, pri Äemu se zahtijevane karbenoid vrste stvaraju iz prethodnika koji sadrži pirazol u prisustvu prikladnog alkena. Jedan takav prethodnik je zastupan od derivata arilsulfonilhidrazona spoja formule (V), tj. spojem formule (VII): 2. The compound of formula (I) can also be obtained by an alternative cyclopropanation strategy, whereby the required carbenoid species are generated from a pyrazole-containing precursor in the presence of a suitable alkene. One such precursor is represented by the arylsulfonylhydrazone derivative of the compound of formula (V), i.e. by the compound of formula (VII):
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gdje je Ar fenil ili naftil od kojih je jedan opcionalno supstituiran sa C1 do C4 alkilom, C1 do C4 alkoksi ili halo, i R1, R3, R5 i R7 su kako je prije definirano za formulu (V). Poželjno, Ar je 4-metilfenil (p-tolil). wherein Ar is phenyl or naphthyl one of which is optionally substituted with C1 to C4 alkyl, C1 to C4 alkoxy or halo, and R1, R3, R5 and R7 are as previously defined for formula (V). Preferably, Ar is 4-methylphenyl (p-tolyl).
Tako spoj formule (VII), u obliku derivata soli alkalnog metala, poželjno litijske soli koja se lako dobiva iz spoja formule (VII) koriÅ”tenjem otopine n-butilitija u heksanu u prikladnom otapalu takvom kao tetrahidrofuran na od oko -78Ā°C do oko sobne temperature, termiÄki se razlaže u prisustvu katalizatora tranzicijskog metala i alkena formule (VIII): Thus, a compound of formula (VII), in the form of an alkali metal salt derivative, preferably a lithium salt readily obtainable from a compound of formula (VII) using a solution of n-butyllithium in hexane in a suitable solvent such as tetrahydrofuran at from about -78Ā°C to about room temperature temperature, it is thermally decomposed in the presence of a transition metal catalyst and an alkene of formula (VIII):
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gdje R2, R4, R6 i R8 su kako je ranije definirano za formulu (I), opcionalno u prikladnom otapalu takvom kao diklorometan i opcionalno pod tlakom. Reakcija se normalno vrÅ”i sa velikim viÅ”kom spoja formule (VIII) na temperaturi od oko sobne do oko 80Ā°C i tlaku od oko 101 kPa (14,7 psi) do oko 2757 kPa (400 psi). Jasno, na poviÅ”enom tlaku, biti Äe potrebno primijeniti posudu visokog tlaka (bomba), Å”to je poželjan postupak za slabo reaktivne alkene. Poželjno, katalizator tranzicijskog metala je rodij(II) u obliku prikladne soli, npr. rodij(II) acetat. wherein R 2 , R 4 , R 6 and R 8 are as previously defined for formula (I), optionally in a suitable solvent such as dichloromethane and optionally under pressure. The reaction is normally carried out with a large excess of the compound of formula (VIII) at a temperature of about room temperature to about 80Ā°C and a pressure of about 101 kPa (14.7 psi) to about 2757 kPa (400 psi). Clearly, at elevated pressure, it will be necessary to apply a high pressure vessel (bomb), which is the preferred procedure for weakly reactive alkenes. Preferably, the transition metal catalyst is rhodium(II) in the form of a suitable salt, eg rhodium(II) acetate.
TipiÄni postupak ukljuÄuje zagrijavanje smjese litijske soli spoja formule (VII), gdje Ar je 4-metilfenil i R1, R3, R5 i R7 su kako je prije definirano za formulu (VII), formulu (VIII) i rodij(II) acetat dimera u nevodenom diklorometanu na od oko 50Ā°C do oko 70Ā°C. A typical procedure involves heating a mixture of the lithium salt of a compound of formula (VII), where Ar is 4-methylphenyl and R1, R3, R5 and R7 are as previously defined for formula (VII), formula (VIII) and rhodium(II) acetate dimer in anhydrous dichloromethane at from about 50Ā°C to about 70Ā°C.
Intermedijeri formule (IV) i (VII), ako nije dalje opisano, mogu se dobiti ili analogno sa postupcima opisanim u poglavlju "Pripreme" ili sa konvencionalnim sintetiÄkim postupcima, prema standardnim knjigama iz organske kemije ili prethodnoj literaturi, iz lako dostupnih polaznih materijala koristeÄi prikladne reagense i reakcijske uvjete. Intermediates of formulas (IV) and (VII), if not further described, can be obtained either analogously to the procedures described in the "Preparations" chapter or by conventional synthetic procedures, according to standard organic chemistry books or previous literature, from readily available starting materials using suitable reagents and reaction conditions.
Osim toga, struÄnjacima Äe biti jasne varijante, i alternative, o onim postupcima opisanim dalje u poglavljima "Primjeri" i "Pripremi" koji omoguÄavaju dobivanje spojeva definiranih formulom (I). In addition, variants, and alternatives, of those procedures described further in the chapters "Examples" and "Preparations" that enable obtaining the compounds defined by formula (I) will be clear to the expert.
Farmaceutski, veterinarski ili agrokulturalno prihvatljive adicijske soli kiseline nekih od spojeva formule (I) mogu se takoÄer dobiti na konvencionalan naÄin. Na primjer, otopina slobodne baze tretira se sa prikladnom kiselinom, ili Äisti u prikladnom otapalu, i rezultirajuÄa sol se izolira ili filtriranjem ili isparavanjem pod sniženim tlakom reakcijskog otapala. Pharmaceutically, veterinary or agroculturally acceptable acid addition salts of some of the compounds of formula (I) can also be obtained in a conventional manner. For example, a solution of the free base is treated with a suitable acid, or purified in a suitable solvent, and the resulting salt is isolated either by filtration or by evaporation under reduced pressure of the reaction solvent.
Spojevi iz izuma, tj. oni iz formule (I), posjeduju antiparazitsku aktivnost kod ljudi, životinja i biljki. Oni su naroÄito korisni u tretiranju ektoparazita. The compounds of the invention, i.e. those of formula (I), possess antiparasitic activity in humans, animals and plants. They are particularly useful in treating ectoparasites.
U vezi primjene spojeva iz izuma kod ljudi, osigurano je: Regarding the application of the compounds of the invention in humans, the following is ensured:
- farmaceutski antiparazitski preparat koji sadrži spoj formule (I), ili njegova farmaceutski prihvatljiva sol, ili njegov farmaceutski prihvatljiv solvat bilo kojeg entiteta, zajedno sa farmaceutski prihvatljivim razblaživaÄem ili nosaÄem, koji se može prilagoditi za lokalno unoÅ”enje; - a pharmaceutical antiparasitic preparation containing a compound of formula (I), or its pharmaceutically acceptable salt, or its pharmaceutically acceptable solvate of any entity, together with a pharmaceutically acceptable diluent or carrier, which can be adapted for local administration;
- spoj formule (I), ili njegova farmaceutski prihvatljiva sol, ili njegov farmaceutski prihvatljiv solvat bilo kojeg entiteta, ili farmaceutski preparat koji sadrži bilo Ŕto od gore navedenog, za primjenu kao lijek; - a compound of formula (I), or its pharmaceutically acceptable salt, or its pharmaceutically acceptable solvate of any entity, or a pharmaceutical preparation containing any of the above, for use as a medicine;
- primjena spoja formule (I), ili njegove farmaceutski prihvatljive soli, ili njegovog farmaceutski prihvatljivog solvata bilo kojeg entiteta, ili farmaceutskog preparata koji sadrži bilo Ŕto od gore navedenog, za proizvodnju lijeka za tretman parazitskog napada; i - application of a compound of formula (I), or its pharmaceutically acceptable salt, or its pharmaceutically acceptable solvate of any entity, or a pharmaceutical preparation containing any of the above, for the production of a drug for the treatment of a parasitic attack; and
- postupak tretiranja parazitskog napada kod ljudi koji obuhvaÄa tretiranje spomenutih ljudi sa djelotvornom koliÄinom spoja formule (I), ili njegove farmaceutski prihvatljive soli, ili njegovog farmaceutski prihvatljivog solvata bilo kojeg entiteta, ili farmaceutskog preparata koji sadrži bilo Å”to od gore navedenog. - a method of treating a parasitic attack in humans comprising treating said humans with an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate thereof of any entity, or a pharmaceutical preparation containing any of the above.
Å to se tiÄe njihove primjene kod životinja, spojevi se mogu unositi sami ili u prikladnoj formulaciji pogodnoj za specifiÄnu razmatranu primjenu, odreÄene vrste životinja domaÄina koje se tretiraju i ukljuÄenog parazita. Metode kojima se spojevi mogu unositi ukljuÄuju oralno unoÅ”enje sa kapsulom, velikom pilulom, tabletom ili lijekom za životinje, lokalno unoÅ”enje kao formulacija lijevanja, mrljanja, umakanja, sprejanja, kreme, Å”ampona ili praha ili, alternativno oni se mogu unositi injekcijom (npr. potkožno, intramuskularno ili intravenozno), ili kao implant. With regard to their use in animals, the compounds may be administered alone or in a suitable formulation suitable for the specific application contemplated, the particular species of host animal being treated and the parasite involved. Methods by which the compounds may be administered include oral administration with a capsule, pill, tablet, or veterinary medicinal product, topical administration as a cast, spot, dip, spray, cream, shampoo, or powder formulation, or alternatively they may be administered by injection (e.g., subcutaneously , intramuscularly or intravenously), or as an implant.
Takve formulacije se dobivaju na konvencionalan naÄin u skladu sa standardnom veterinarskom praksom. Tako se kapsule, velike pilule ili tablete mogu dobiti mijeÅ”anjem aktivnog sastojka sa prikladnim fino podijeljenim razblaživaÄem ili nosaÄem koji dodatno sadrži agens razgraÄivanja i/ili vezivanja takav kao Å”krob, laktoza, talk ili magnezij stearat, itd. Oralni lijekovi se dobivaju otapanjem ili suspendiranjem aktivnog sastojka u prikladnoj sredini. Formulacije lijevanja ili mrljanja mogu se dobiti otapanjem aktivnog sastojka u prihvatljivom tekuÄem nosaÄu takvom kao butil digol, tekuÄi parafin ili neispariv ester, opcionalno sa dodavanjem isparive komponente takve kao propan-2-ol. Alternativno, formulacije lijevanja, mrljanja ili sprejanja mogu se dobiti dekapsuliranjem, radi ostavljanja ostatka aktivnog agensa na povrÅ”ini životinje. Formulacije injekcija mogu se dobiti u obliku sterilne otopine koja može sadržavati druge supstance, na primjer dosta soli ili glukoze da bi otopina bila izotoniÄna sa krvlju. Prihvatljivi tekuÄi nosaÄi ukljuÄuju biljna ulja takva kao sezamovo ulje, gliceride takve kao triacetin, estere takve kao benzil benzoat, izopropil miristat i derivate masne kiseline propilen glikola, isto kao i organska otapala takva kao pirolidin-2-jedan i glicerol formal. Formulacije se dobivaju otapanjem ili suspendiranjem aktivnog sastojka u tekuÄem nosaÄu tako da finalna koncentracija sadrži od 0,01 do 10 % mase aktivnog sastojka. Such formulations are obtained in a conventional manner in accordance with standard veterinary practice. Thus, capsules, large pills or tablets can be obtained by mixing the active ingredient with a suitable finely divided diluent or carrier that additionally contains a disintegrating and/or binding agent such as starch, lactose, talc or magnesium stearate, etc. Oral drugs are obtained by dissolving or suspending the active ingredient in a suitable environment. Cast or spot formulations may be obtained by dissolving the active ingredient in an acceptable liquid carrier such as butyl digol, liquid paraffin or a non-volatile ester, optionally with the addition of a volatile component such as propan-2-ol. Alternatively, pour, spot or spray formulations may be obtained by decapsulation, to leave a residue of the active agent on the surface of the animal. Injection formulations may be obtained as a sterile solution which may contain other substances, for example enough salt or glucose to make the solution isotonic with blood. Acceptable liquid carriers include vegetable oils such as sesame oil, glycerides such as triacetin, esters such as benzyl benzoate, isopropyl myristate, and fatty acid derivatives of propylene glycol, as well as organic solvents such as pyrrolidine-2-one and glycerol formal. Formulations are obtained by dissolving or suspending the active ingredient in a liquid carrier so that the final concentration contains from 0.01 to 10% by weight of the active ingredient.
Ove formulacije mijenjati Äe se zavisno od mase aktivnog spoja sadržanog u njima, zavisno o vrsti životinje domaÄina koja se tretira, ozbiljnosti i tipa infekcije i tjelesne težine domaÄina. Za parenteralno, lokalno i oralno unoÅ”enje, tipiÄni dozni opsezi aktivnog sastojka su 0,01 do 100 mg po kg tjelesne težine životinje. Poželjni opseg je 0,1 do 10 mg po kg. These formulations will vary depending on the mass of active compound contained in them, depending on the type of host animal being treated, the severity and type of infection and the body weight of the host. For parenteral, local and oral administration, typical dosage ranges of the active ingredient are 0.01 to 100 mg per kg of animal body weight. The preferred range is 0.1 to 10 mg per kg.
Kao alternativa spojevi se mogu unositi sa životinjskom hranom, a za ovu svrhu može se dobiti koncentrirani dodatak hrane ili premiks za mijeŔanje sa normalnom životinjskom hranom. As an alternative, the compounds can be introduced with animal feed, and for this purpose a concentrated feed supplement or premix can be obtained for mixing with normal animal feed.
Spojevi iz izuma su korisni za kontrolu artropodnih bolesti. Oni mogu biti, naroÄito, koriÅ”teni na podruÄju veterinarske medicine, stoke za poljoprivredu i održavanje javnog zdravlja: protiv artropoda koji su parazitski interno ili eksterno prema kralježnjacima, naroÄito toplokrvnim kralježnjacima, ukljuÄujuÄi Äovjeka i domaÄe životinje takve kao goveda, ovce, koze, konji, svinje, živina, psi, maÄke i ribe, na primjer Acarina, ukljuÄujuÄi krpelje (npr. Ixodes spp., Boophilus spp., npr. Boophilus microplus, Amblyomma spp., Hyalomma spp., Rhipicephalus spp., npr. Rhipicephalus appendiculatus, Haemaphysalis spp., Dermacentor spp., Ornithodorus spp. (npr. Omithodorus moubata), crve (npr. Damalinia spp., Dermanyssus gallinae, Sarcoptes spp. npr. Sarcoptes scabiei, Psoroptes spp., Chorioptes spp., Demodex spp., Eutrombicula spp.); Diptera (npr. Aedes spp., Anopheles spp., Muscidae spp. tj. Stomoxys calcitrans i Haematobia irritans, Hypoderma spp., Gastrophilus spp., Simulium spp.); Hemiptera (npr. Triatoma spp.); Phthiraptera (npr. Damalinia spp., Linognathus spp.); Siphonaptera (npr. Ctenocephalides spp.); Dictyoptera (npr. Periplaneta spp., Blatella spp. ) i Hymenoptera (npr. Monomorium pharaonis); u zaÅ”titi skladiÅ”tenih proizvoda, na primjer žitarica ukljuÄujuÄi žito i braÅ”no, kikiriki, životinjsku hranu, drvenu graÄu i proizvode za kuÄanstvo , npr. tepisi i tekstili, protiv napada artropoda, preciznije kukaca ukljuÄujuÄi žižak, moljce i crve, na primjer Ephestia spp. (moljac u braÅ”nu), Anthrenus spp. (kukci u tepihu), Tribolium spp. (kukci u braÅ”nu), Sitophilus spp. (kukci u žitu) i Acarus spp. (crvi); u kontroli žohara, mrava i termita i sliÄnih artropodnih Å”tetoÄina u napadnutim domaÄim i industrijskim gore iznijetim materijalima; u kontroli larvi moskito komaraca u vodenim tokovima, izvorima, rezervoarima i drugim tekuÄim ili stajaÄim vodama; u tretmanu temelja, strukture i zemljiÅ”ta za prevenciju napada termita na zgrade, na primjer Reticulitermes spp., Heterotermes spp., Coptotermes spp.; u poljoprivredi protiv odraslih, larvi i jaja od Lepidoptera (leptiri i moljci) npr. Heliothis spp. takav kao Heliothis virescens (crv na pupoljku duhana), Heliothis i Heliothis zea, Spodoptera spp. takav kao S. exempta, S. littoralis (crv egipatskog pamuka), S. eridania (južni "vojni"crv), Mamestra configurata ("vojni" crv Äipke), Earis spp., npr. E. insulana (egipatski crv sjemenog tobolca pamuka), Pectinophora spp., npr. Pectinophora gossypiella (ružiÄasti crv sjemenog tobolca pamuka), Ostrinia spp. takav kao . nubilalis (europski žitni kukac), Trichoplusia ni (kupusova gusjenica), Pieris spp. (kupusovi crvi), Laphyqma spp. ("vojni" crvi), Agrotis i Amathes spp. (gusjenice koje odgrizaju mlade biljke u razini zemlje), Wiseana spp. (porina moljac), Chilo spp. (kukac stabljike riže), Tryporyza spp. i Diatraea spp. (kukci Å”eÄerne trske i kukci riže), Sparganothis pilleriana (moljac bobice grožÄa), Cydia pomonella (moljac jabuke), Archips spp. (tortrix moljci voÄnog drveta), Plutella xylostella (moljac crni dijamant); protiv odraslih i larvi od Coleoptera (kukci) npr. Hypothenemus hampei (kukac zrna kave), Hylesinus spp. (kukci kore drveÄa), Anthonomus grandis (žižak pamuka), Acalymma spp. (kukci krastavca), Lema spp., Psylliodes spp., Leptinotarsa decemlineata (kukac Colorado krumpira), Diabrotica spp. (crv žitnog korijena), Gonocephalum spp. (lažne liÄinke klisnjaka), Agriotes spp. (liÄinke klisnjaka), Dermolepida i Heteronychus spp. (bijeli crvi), Phaedon cochleariae (kukac senfa), Lissorhopturus oryzophilus (vodeni kukac riže), Melioethes spp. (kukci peluda), Ceutorhynchus spp., Rhynchophorus i Cosmopolites spp. (žiÅ”ci korijena); protiv Hemiptera npr. Psylla spp., Bemisia spp., Trialeurodes spp., Aphis spp., Myzus spp., Megoura viciae, Phylloxera spp., Adelges spp., Phorodon humuli (insekt damaÅ”kog hmelja), Aeneolamia spp., Nephotettix spp. (skakavci lista riže), Empoasca spp., Nilaparvata spp., Perkinsiella spp., Pyrilla spp., Aonidiella spp. (crvene ljuske), Coccus spp., Pseucoccus spp., Helopeltis spp. (moskito stjenice), Lygus spp., Dysdercus spp., Oxycarenus spp., Nezara spp., Nymenoptera npr. Athalia spp. i Cephus spp. (ose biljarice), Atta spp. (mravi koji sijeku listove), Diptera npr. Hylemyia spp. (muhe korijena), Atherigona spp. i Chlorops spp. (muhe mladica), Phytomyza spp. (buÅ”aÄi lista), Ceratitis spp. (voÄne muhe), Thysanoptera kao Å”to su Thrips tabaci, Orthoptera kao Å”to su Locusta i Schistocerca spp. (skakavci) i zrikavci npr. Gryllus spp. i Acheta spp., Collembola npr. Sminthurus spp. i Onychiurus spp. (insketi bez krila), Isoptera npr. Odontotermes spp. (termiti), Dermaptera npr. Foficula spp. (insekti) i takoÄer protiv drugih artropoda od agrokulturalnog znaÄaja kao Å”to su Acari (crvi) npr. Tetranychus spp., Panonychus spp. i Bryobia spp. (pauci crvi), Eriophyes spp. (crvi Å”iÅ”arice), Polyphacotarsonemus spp., Blaniulus spp. (stonoge), Scutigerella spp. (insekti), Oniscus spp. (uÅ”i drveta) i Triops spp. (ljuskari). The compounds of the invention are useful for the control of arthropod diseases. They can be, in particular, used in the field of veterinary medicine, livestock for agriculture and public health maintenance: against arthropods that are parasitic internally or externally to vertebrates, especially warm-blooded vertebrates, including humans and domestic animals such as cattle, sheep, goats, horses, pigs, poultry, dogs, cats and fish, e.g. Acarina, including ticks (e.g. Ixodes spp., Boophilus spp., e.g. Boophilus microplus, Amblyomma spp., Hyalomma spp., Rhipicephalus spp., e.g. Rhipicephalus appendiculatus, Haemaphysalis spp., Dermacentor spp., Ornithodorus spp. (eg Omitodorus moubata), worms (eg Damalinia spp., Dermanyssus gallinae, Sarcoptes spp. eg Sarcoptes scabiei, Psoroptes spp., Chorioptes spp., Demodex spp., Eutrombicula spp. .); Diptera (e.g. Aedes spp., Anopheles spp., Muscidae spp. i.e. Stomoxys calcitrans and Haematobia irritans, Hypoderma spp., Gastrophilus spp., Simulium spp.); Hemiptera (e.g. Triatoma spp.); Phthiraptera ( eg Damalinia spp., Lin ognathus spp.); Siphonaptera (eg Ctenocephalides spp.); Dictyoptera (eg Periplaneta spp., Blatella spp. ) and Hymenoptera (eg Monomorium pharaonis); in the protection of stored products, for example cereals including grain and flour, peanuts, animal feed, timber and household products, for example carpets and textiles, against attack by arthropods, more specifically insects including weevils, moths and worms, for example Ephestia spp. ( flour moth), Anthrenus spp. (carpet bugs), Tribolium spp. (flour bugs), Sitophilus spp. (grain insects) and Acarus spp. (worms); in the control of cockroaches, ants and termites and similar arthropod pests in the infested domestic and industrial materials listed above; in the control of mosquito larvae in water courses, springs, reservoirs and other running or stagnant water; in the treatment of foundations, structures and land for the prevention of termite attacks on buildings, for example Reticulitermes spp., Heterotermes spp., Coptotermes spp.; in agriculture against adults, larvae and eggs of Lepidoptera (butterflies and moths) e.g. Heliothis spp. such as Heliothis virescens (tobacco budworm), Heliothis and Heliothis zea, Spodoptera spp. such as S. exempta, S. littoralis (worm Egyptian cotton), S. eridania (southern "army" worm), Mamestra configurata ("army" lace worm), Earis spp., e.g. E. insulana (Egyptian cotton bollworm), Pectinophora spp., e.g. Pectinophora gossypiella (pink cotton bollworm), Ostrinia spp. such as . nubilalis (European grain bug), Trichoplusia ni (cabbage caterpillar), Pieris spp. (cabbage worms), Laphyqma spp. ("army" worms), Agrotis and Amathes spp. (caterpillars that bite off young plants at ground level), Wiseana spp. (porina moth), Chilo spp. (rice stem bug), Tryporyza spp. and Diatraea spp. (sugarcane bugs and rice bugs), Sparganothis pilleriana (grape berry moth), Cydia pomonella (apple moth), Archips spp. tortrix fruit tree moths), Plutella xylostella (black diamond moth); against adults and larvae of Coleoptera (insects) eg Hypothenemus hampei (coffee bean bug), Hylesinus spp. (tree bark beetles), Anthonomus grandis (cotton weevil), Acalymma spp. (cucumber bugs), Lema spp., Psylliodes spp. , Leptinotarsa decemlineata (Colorado potato bug), Diabrotica spp. (cereal rootworm), Gonocephalum spp. (false grasshopper larvae), Agriotes spp. (grasshopper larvae), Dermolepida and Heteronychus spp. (white worms), Phaedon cochleariae (mustard bug ), Lissorhopturus oryzophilus (aquatic rice bug), Melioethes spp. (pollen bugs), Ceutorhynchus spp., Rhynchophorus and Cosmopolites spp. (root borers); against Hemiptera, eg Psylla spp., Bemisia spp., Trialeurodes spp., Aphis spp., Myzus spp., Megoura viciae, Phylloxera spp., Adelges spp., Phorodon humuli (damask hop insect), Aeneolamia spp., Nephotettix spp. (rice leafhoppers), Empoasca spp., Nilaparvata spp., Perkinsiella spp., Pyrilla spp., Aonidiella spp. (red scales), Coccus spp., Pseucoccus spp., Helopeltis spp. (mosquito bugs), Lygus spp., Dysdercus spp., Oxycarenus spp., Nezara spp., Nymenoptera eg Athalia spp. and Cephus spp. (billiard wasps), Atta spp. (leaf cutter ants), Diptera eg Hylemyia spp. (root flies), Atherigona spp. ... and Chlorops spp. spp. and Acheta spp., Collembola e.g. Sminthurus spp. and Onychiurus spp. (wingless insects), Isoptera e.g. Odontotermes spp. (termites), Dermaptera e.g. Foficula spp. (insects) and also against other arthropods of agrocultural importance such as Acari (worms) eg Tetranychus spp., Panonychus spp. and Bryobia spp. (spider worms), Eriophyes spp. (cone worms), Polyphacotarsonemus spp., Blaniulus spp. (millipedes), Scutigerella spp. (insects), Oniscus spp. (wood lice) and Triops spp. (scalers).
Spojevi iz ovog izuma takoÄer su korisni u kontroli artropodnih Å”tetoÄina biljaka. Aktivni spoj se opÄenito primjenjuje na mjestu gdje se napad artropoda treba kontrolirati u koliÄini od oko 0,005 kg do oko 25 kg aktivnog spoja po hektaru (ha) na tretiranom mjestu, poželjno 0,02 do 2 kg/ha. Pod idealnim uvjetima, ovisno od napasti koju treba kontrolirati, manja koliÄina može ponuditi odgovarajuÄu zaÅ”titu. S druge strane, nepovoljni vremenski uvjeti i drugi faktori mogu zahtijevati da se aktivni sastojak koristi u veÄim iznosima. Za lisnu primjenu, može se koristiti koliÄina od 0,01 do 1 kg/ha. The compounds of this invention are also useful in the control of arthropod pests of plants. The active compound is generally applied to the site where arthropod infestation is to be controlled in an amount of about 0.005 kg to about 25 kg of active compound per hectare (ha) of the treated site, preferably 0.02 to 2 kg/ha. Under ideal conditions, depending on the infestation to be controlled, a smaller amount may offer adequate protection. On the other hand, adverse weather conditions and other factors may require the active ingredient to be used in larger amounts. For foliar application, an amount of 0.01 to 1 kg/ha can be used.
Kada je Å”tetoÄina razvijena u zemlji, formulacija koja sadrži aktivni spoj se raspodjeljuje ravnomjerno preko podruÄja koje se tretira na bilo koji prikladan naÄin. Primjena se može izvrÅ”iti, ako se želi, na polje ili podruÄje rasta ljetine opÄenito, ili u blizini sjemena ili biljke radi zaÅ”tite od napada. Aktivna komponenta može se sprati u zemlju rasprÅ”ivanjem vode preko podruÄja ili se može ostaviti prirodnom djelovanju kiÅ”e. Za vrijeme ili nakon primjene, formulacija se može, ako se želi, raspodijeliti mehaniÄki u zemlju, na primjer oranjem ili tanjuranjem. Primjena može biti prije saÄenja, tokom saÄenja, nakon saÄenja ali prije klijanja, ili nakon klijanja. When the pest is developed in the soil, the formulation containing the active compound is distributed evenly over the area to be treated in any suitable manner. Application may be made, if desired, to the field or area of summer growth in general, or near the seed or plant to protect against attack. The active component can be washed into the ground by spraying water over the area or it can be left to the natural action of rain. During or after application, the formulation can, if desired, be spread mechanically into the soil, for example by plowing or discing. Application can be before planting, during planting, after planting but before germination, or after germination.
Spojevi iz izuma vrijedni su u kontroli Å”tetoÄina koji se hrane u dijelovima biljke udaljenim od mjesta primjene, npr. insekti koji se hrane listom mogu biti ubijeni primjenom predmetnih spojeva na korijenima. Dalje, spojevi mogu reducirati napade na biljku pomoÄu efekata gaÄenja ili odbijanja ishrane. The compounds of the invention are valuable in controlling pests that feed on parts of the plant remote from the application site, eg leaf-feeding insects can be killed by applying the subject compounds to the roots. Further, the compounds may reduce attacks on the plant through disgust or repulsion effects.
Spojevi iz izuma od naroÄitog su znaÄaja u zaÅ”titi polja, stoÄne hrane, plantaža, staklenika, ljetine voÄnjaka i vinograda, ili ukrasnih biljaka, i plantaže i Å”umskih drveÄa, na primjer žitarica (kao Å”to su kukuruz, pÅ”enica, riža, trava), pamuka, duhana, povrÄa i salate (kao Å”to su grah, kelj, salata, luk, paradajz i papar), ljetine polja (kao Å”to su krumpir, Å”eÄerna repa, zemni orah, soja, sjeme uljane repice), Å”eÄerne trske, trave i stoÄne hrane (kao Å”to su kukuruz, trava, djetelina), plantaže (kao Å”to su Äaj, kava, kakao, banana, uljana palma, kokosov orah, guma, mirodije), voÄnjaka i lugova (kao Å”to su voÄe sa koÅ”ticom i zrnasto voÄe, limun, kivi, avokado, mango, maslina i orah), vinograda, ukrasnih biljaka, cvijeÄa i grmova pod staklom, u vrtovima i u parkovima, i Å”umskih drveÄa (oba listopadno i zimzeleno) u Å”umama, plantažama i rasadnicima. The compounds of the invention are of particular importance in the protection of fields, fodder, plantations, greenhouses, summer orchards and vineyards, or ornamental plants, and plantations and forest trees, for example cereals (such as corn, wheat, rice, grass), cotton , tobacco, vegetables and salads (such as beans, kale, lettuce, onions, tomatoes and peppers), summer fields (such as potatoes, sugar beets, peanuts, soybeans, rapeseed), sugar cane, grasses and livestock food (such as corn, grass, clover), plantations (such as tea, coffee, cocoa, banana, oil palm, coconut, rubber, spices), orchards and lye (such as stone fruits and grain fruits, lemon, kiwi, avocado, mango, olive and walnut), vineyards, ornamental plants, flowers and shrubs under glass, in gardens and parks, and forest trees (both deciduous and evergreen) in forests, plantations and nurseries.
Oni su isto tako vrijedni u zaÅ”titi drveÄa (stojeÄeg, oborenog, obraÄenog, skladiÅ”tenog ili graÄevinskog) od napada osa biljarica (npr. Urocerus), kukaca (npr. scolytids, platypodids, lyctids, bostrychids, cerambycids, anobiids) ili termita (npr. Reticulitermes spp., Heterotermes spp., Coptotermes spp.). They are also valuable in protecting trees (standing, felled, cultivated, stored or construction) from attacks by wasps (e.g. Urocerus), insects (e.g. scolytids, platypodids, lyctids, bostrychids, cerambycids, anobiids) or termites (e.g. Reticulitermes spp., Heterotermes spp., Coptotermes spp.).
Dalje, oni imaju primjene u zaÅ”titi skladiÅ”tenih proizvoda kao Å”to su žita, voÄe, orasi, mirodije i duhan, ili cijelih, samljevenih ili sjedinjenih u proizvodima, od napada moljaca, kukaca i crva. TakoÄer zaÅ”tiÄeni su skladiÅ”teni životinjski proizvodi kao Å”to su kože, dlaka, vuna i perje u prirodnom ili preraÄenom obliku (npr. kao tepisi ili tekstil) od napada moljaca i kukaca, kao Å”to su meso i riba od napada kukaca, crva i muha. Furthermore, they have applications in the protection of stored products such as grain, fruit, nuts, spices and tobacco, or whole, ground or combined in products, against attack by moths, insects and worms. Also protected are stored animal products such as skins, hair, wool and feathers in natural or processed form (eg as carpets or textiles) from moths and insects, such as meat and fish from insects, worms and flies.
Spojevi iz izuma su vrijedni u kontroli ili artropodima koji su Å”tetni, ili rasijani ili djeluju kao prenosioci bolesti kod Äovjeka i domaÄih životinja, na primjer onih prije spomenutih, i specifiÄnije u kontroli krpelja, crva, uÅ”i, buha, muÅ”ica i oÅ”trih, dosadnih i napasnih muha. Oni su naroÄito korisni u kontroliranju artropoda koji se susreÄu unutar domaÄih životinja domaÄina koji se hrane tu ili na koži ili siÅ”u krv životinja, za koju svrhu se oni mogu unositi oralno, parenteralno, perkožno ili mjesno. The compounds of the invention are valuable in the control or arthropods that are harmful, or spread, or act as vectors of disease in humans and domestic animals, for example those previously mentioned, and more specifically in the control of ticks, worms, lice, fleas, flies and sharp, annoying and bait flies. They are particularly useful in controlling arthropods found inside domestic animal hosts that feed there or on the skin or suck the blood of animals, for which purpose they can be introduced orally, parenterally, percutaneously or locally.
Zato, prema daljem aspektu izuma, osigurana je veterinarska ili agrokulturalna formulacija koja sadrži spoj formule (I), ili njegovu veterinarski ili agrokulturalno prihvatljivu sol, ili njegov veterinarski ili agrokulturalno prihvatljiv solvat bilo kojeg entiteta, zajedno sa veterinarski ili agrokulturalno prihvatljivim razblaživaÄem ili nosaÄem. Poželjno, formulacija je prilagoÄena za mjesno unoÅ”enje. Therefore, according to a further aspect of the invention, there is provided a veterinary or agrocultural formulation comprising a compound of formula (I), or a veterinary or agroculturally acceptable salt thereof, or a veterinary or agroculturally acceptable solvate thereof of any entity, together with a veterinary or agroculturally acceptable diluent or carrier. Preferably, the formulation is adapted for topical administration.
Izum dalje osigurava spoj formule (I), ili njegovu veterinarski ili agrokulturalno prihvatljivu sol, ili njegov veterinarski ili agrokulturalno prihvatljiv solvat bilo kojeg entiteta, ili veterinarski ili agrokulturalno prihvatljivu formulaciju koja sadrži bilo Ŕto od gore navedenog, za primjenu kao antiparazitsko sredstvo. The invention further provides a compound of formula (I), or a veterinary or agroculturally acceptable salt thereof, or a veterinary or agroculturally acceptable solvate thereof of any entity, or a veterinary or agroculturally acceptable formulation containing any of the above, for use as an antiparasitic agent.
On takoÄer osigurava metodu za tretiranje parazitske napasti na mjestu, koji obuhvaÄa tretman mjesta sa djelotvornom koliÄinom spoja formule (I), ili njegove veterinarski ili agrokulturalno prihvatljive soli, ili njegovog veterinarski ili agrokulturalno prihvatljivog solvata bilo kojeg entiteta, ili veterinarski ili agrokulturalno prihvatljive formulacije koji sadrže bilo Å”to od gore navedenog. It also provides a method for treating a parasitic infestation at a site, comprising treating the site with an effective amount of a compound of formula (I), or a veterinary or agroculturally acceptable salt thereof, or a veterinary or agroculturally acceptable solvate thereof of any entity, or a veterinary or agroculturally acceptable formulation which contain any of the above.
Poželjno, mjesto je koža ili krzno životinje, ili povrŔina biljke, ili zemljiŔte oko biljke koja se tretira. Preferably, the site is the skin or fur of an animal, or the surface of a plant, or the soil around the plant being treated.
Treba primijetiti da referenca na tretman ukljuÄuje profilaksu isto kao i ublažavanje i/ili lijeÄenje utvrÄenih simptoma parazitske infekcije. It should be noted that reference to treatment includes prophylaxis as well as alleviation and/or treatment of established symptoms of parasitic infection.
Test za insekticidnu aktivnost Test for insecticidal activity
Odrasle muhe (Stomoxys calcitrans) sakupe se i anestetiziraju koriÅ”tenjem CO2. Otopina acetona (1 Āµl) koja sadrži test-spoj primjenjuje se direktno na prsni dio svake muhe i zatim se muhe postave pažljivo u cijev od 50 ml pokrivenu sa vlažnom gazom da se oporave od CO2. Negativne kontrole imaju aceton (1 Āµl) odmjeren na njih. Smrtnost je odreÄena 24 sata nakon doziranja. Tablica 1 ilustrira in vitro aktivnost odabiranja spojeva iz izuma protiv odraslih Stomoxys calcitrans. Doziranja potrebna za dobivanje 100 %-ne smrtnosti data su u posljednjoj koloni kao Āµg/muha. Adult flies (Stomoxys calcitrans) are collected and anesthetized using CO2. An acetone solution (1 Āµl) containing the test compound is applied directly to the thorax of each fly and then the flies are placed carefully in a 50 ml tube covered with moist gauze to recover from CO2. Negative controls have acetone (1 Āµl) metered onto them. Mortality was determined 24 hours after dosing. Table 1 illustrates the in vitro activity of selected compounds of the invention against Stomoxys calcitrans adults. Doses required to obtain 100% mortality are given in the last column as Āµg/fly.
TABLICA 1 TABLE 1
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Test za aktivnost protiv pregalja Test for anti-scalding activity
Doza od 10 Āµg/cm2 je napravljena ravnomjernim kapanjem 0,5 ml od 1 mg/ml otopine test-spoja u prikladnom otapalu kao Å”to je aceton ili etanol na Whatman No. 1 ā¢ filter papir odsjeÄen na veliÄinu od 8 Ć 6,25 cm. Kada se osuÅ”i, papir se savije na polovinu, zaÄepe se 2 strane sa ureÄajem za krimpiranje i postavi se u Kilner posudu koja sadrži krpu od pamuÄnih niti ovlaženu sa vodom. Posuda se zatim zaÄepi i postavi na 25 Ā°C tokom 24 sata. Dalje, približno 50 Boophilus microplus larvi se uvodi na omot tretiranog papira koji se zatim krimpira duž treÄe strane radi postizanja kompletnog zatvaranja. Omot papira se vraÄa u Kilner posudu, koja se zaÄepi i postavlja na 25 Ā°C tokom daljnjih 48 sati. Papiri se zatim uklanjaju i odreÄuje se smrtnost. Negativne kontrole se osiguraju tretiranjem prikladno isjeÄenog filter papira sa samo 0,5 ml otopine i praÄenjem istog postupka. Aktivnost u drugim dozama dobiva se mijenjanjem koncentracije test spoja. A dose of 10 Āµg/cm2 was made by uniformly dropping 0.5 ml of a 1 mg/ml solution of the test compound in a suitable solvent such as acetone or ethanol onto a Whatman No. 1 ā¢ filter paper cut to a size of 8 x 6.25 cm. When dry, the paper is folded in half, 2 sides are closed with a crimping device and placed in a Kilner container containing a cotton thread cloth moistened with water. The container is then closed and placed at 25 Ā°C for 24 hours. Next, approximately 50 Boophilus microplus larvae are introduced onto a treated paper wrapper which is then crimped along the third side to achieve complete closure. The paper wrapper is returned to the Kilner dish, which is stoppered and placed at 25 Ā°C for a further 48 hours. The papers are then removed and mortality is determined. Negative controls are provided by treating appropriately cut filter paper with only 0.5 ml of solution and following the same procedure. Activity in other doses is obtained by changing the concentration of the test compound.
Tablica 2 ilustrira in vitro aktivnost izabranih spojeva iz izuma protiv Boophilus microplus larvi. Doziranja potrebna da se dobije 100 %-na smrtnost data su u posljednjoj koloni kao Āµg/cm2. Table 2 illustrates the in vitro activity of selected compounds of the invention against Boophilus microplus larvae. Doses required to obtain 100% mortality are given in the last column as Āµg/cm2.
TABLICA 2 TABLE 2
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Sinteza spojeva iz izuma i intermedijera za njihovu primjenu ilustrirana je slijedeÄim primjerima i dobivanjima. The synthesis of the compounds of the invention and intermediates for their application is illustrated by the following examples and preparations.
ToÄke topljenja su odreÄene koriÅ”tenjem Gallenkamp aparata za toÄku topljenja i nisu korigirane. Melting points were determined using a Gallenkamp melting point apparatus and are uncorrected.
Spektralni podaci nuklearne magnetne rezonance (NMR) dobiveni su koriÅ”tenjem Bruker AC300 ili AM300 spektrometra, pri Äemu su zapaženi kemijski pomaci (Ī“) bili dosljedni sa predloženim strukturama. Nuclear magnetic resonance (NMR) spectral data were obtained using a Bruker AC300 or AM300 spectrometer, with the observed chemical shifts (Ī“) being consistent with the proposed structures.
Spektralni maseni (MS) podaci su dobiveni na Finnigan Mat. TSQ 7000 ili na Fisons Instruments Trio 1000 spektrometru. IzraÄunati i primijeÄeni odreÄeni ioni pokazuju na izotopski preparat najmanje mase. Mass spectral (MS) data were obtained on a Finnigan Mat. TSQ 7000 or on a Fisons Instruments Trio 1000 spectrometer. The calculated and observed specific ions point to the isotopic preparation of the lowest mass.
HPLC oznaÄava visoko provoÄenje tekuÄe kromatografije. HPLC stands for high performance liquid chromatography.
Sobna temperatura oznaÄava 20 do 25 Ā°C. Room temperature means 20 to 25 Ā°C.
Primjer 1 Example 1
5-amino-3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 5-amino-3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Jako izmijeÅ”ana smjesa naslovnog spoja pripreme 2 (1,0 g), bromoforma (13 ml), benziltrietilamonij klorida (0,075 g), 60 % vodene otopine natrij hidroksida (2 ml), diklorometana (12 ml) i etanola (0,5 ml) zagrijavana je pod refluksom tokom 19 dana, zatim je ostavljena da se ohladi i razblažena je sa vodom. Izdvojena organska faza je primijenjena na stupac silikagela (10 g) i izvrÅ”ena je elucija sa diklorometanom. Sirovi proizvod dobiven iz odgovarajuÄih frakcija je proÄiÅ”Äen obrnutom fazom HPLC na C18 silicija , koristeÄi acetonitril:voda:metanol (50:40:10) kao eluanta, radi dobivanja spoja iz naslova kao sasvim bijeli Ävrsti proizvod, t.t. 178-179 Ā°C. A highly stirred mixture of the title compound of Preparation 2 (1.0 g), bromoform (13 mL), benzyltriethylammonium chloride (0.075 g), 60% aqueous sodium hydroxide (2 mL), dichloromethane (12 mL), and ethanol (0.5 mL) ) was heated under reflux for 19 days, then allowed to cool and diluted with water. The separated organic phase was applied to a silica gel column (10 g) and eluted with dichloromethane. The crude product obtained from the appropriate fractions was purified by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (50:40:10) as eluent, to give the title compound as an off-white solid, m.p. 178-179 Ā°C.
Ī“ (CDCl3): 2,28 (d, 2H); 2,61 (t, 1H); 3,80 (br.s, 2H); 7,8 (s, 2H). Ī“ (CDCl 3 ): 2.28 (d, 2H); 2.61 (t, 1H); 3.80 (number s, 2H); 7.8 (s, 2H).
MS (termosprej): M/Z [M+H] 516,4; MS (thermospray): M/Z [M+H] 516.4;
C14H7Br2Cl2F3N4 + H zahtijeva 516,84. C14H7Br2Cl2F3N4 + H requires 516.84.
Primjer 2 Example 2
3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Etanol (0,1 ml) i otopina natrij hidroksida (0,29 g) u vodi (0,5 ml) dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 4 (0,6 g) i bromoforma (1,83 g) u diklorometanu (2 ml), praÄeno benziltrietilamonij kloridom (0,01 g). Reakcijska smjesa je mijeÅ”ana, sukcesivno, na sobnoj temperaturi tokom 18 sati, na 50 Ā°C tokom 5 sati, na sobnoj temperaturi tokom 48 sati, na 50 Ā°C tokom 4 sata i na sobnoj temperaturi tokom 18 sati, zatim je podijeljena izmeÄu diklorometana (100 ml) i vode (100 ml). Organska faza je izdvojena, osuÅ”ena (MgSO4) i isparena pod reduciranim tlakom radi dobivanja ulja koje je proÄiÅ”Äeno kromatografijom stupca na silikagelu (10 g), koristeÄi heksan:diklorometan (3:7) kao eluant, praÄeno kristalizacijom zahtjevanog materijala iz heksana. Spoj iz naslova je tako dobiven kao bijeli Ävrsti proizvod, t.t. 121-123 Ā°C. Ethanol (0.1 ml) and a solution of sodium hydroxide (0.29 g) in water (0.5 ml) were added to a mixed solution of the title compound 4 (0.6 g) and bromoform (1.83 g) in dichloromethane (2 ml), followed by benzyltriethylammonium chloride (0.01 g). The reaction mixture was stirred, successively, at room temperature for 18 hours, at 50 Ā°C for 5 hours, at room temperature for 48 hours, at 50 Ā°C for 4 hours and at room temperature for 18 hours, then it was partitioned between dichloromethane ( 100 ml) and water (100 ml). The organic phase was separated, dried (MgSO4) and evaporated under reduced pressure to give an oil which was purified by column chromatography on silica gel (10 g), using hexane:dichloromethane (3:7) as eluent, followed by crystallization of the required material from hexane. The title compound was thus obtained as a white solid, m.p. 121-123 Ā°C.
Ī“ (CDCl3): 2,02 (t, 1H); 2,34 (dd, 1H); 2,88 (dd, 1H); 7,53 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 2.02 (t, 1H); 2.34 (dd, 1H); 2.88 (dd, 1H); 7.53 (s, 1H); 7.78 (s, 2H).
MS (termosprej): M/Z [M+NH4] 518,9. MS (thermospray): M/Z [M+NH 4 ] 518.9.
C14H6Br2Cl2F3N3 + NH4 zahtijeva 518,86. C14H6Br2Cl2F3N3 + NH4 requires 518.86.
Primjeri 3A i 3B Examples 3A and 3B
A. (-)-3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol i A. (-)-3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole and
B. (+)-3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol B. (+)-3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Spoj iz naslova iz primjera 2 (28,5 mg) rastopljen je hiralnim HPLC koristeÄi Chiralpak ā¢ AD stupca (25 cm Ć 25 cm), smjesu heksan:propan-2-ola (93:7) kao eluanta i brzine elucije od 9 ml/minuti. The title compound from Example 2 (28.5 mg) was resolved by chiral HPLC using a Chiralpak ā¢ AD column (25 cm Ć 25 cm), a mixture of hexane:propan-2-ol (93:7) as eluent and an elution rate of 9 ml /minutes.
(-)-enantiomer (A) je prvo eluciran i dobiven je kao bijeli Ävrsti kristalni proizvod, t.t. 132,5-135 Ā°C. The (-)-enantiomer (A) was eluted first and was obtained as a white solid crystalline product, m.p. 132.5-135 Ā°C.
[image] -42,54 Ā° (c=1,5 mg/ml, metanol). [image] -42.54 Ā° (c=1.5 mg/ml, methanol).
(+)-enantiomer (B) je eluciran drugi i dobiven je kao bijeli Ävrsti kristalni proizvod, t.t. 132,5-134 Ā°C. The (+)-enantiomer (B) eluted second and was obtained as a white solid crystalline product, m.p. 132.5-134 Ā°C.
[image] +44,02 Ā° (c=3,5 mg/ml, metanol). [image] +44.02 Ā° (c=3.5 mg/ml, methanol).
PomoÄu kristalografske analize X-zraka odreÄeno je da ovaj posljednji enantiomer posjeduje R-konfiguraciju. X-ray crystallographic analysis determined that this last enantiomer has the R-configuration.
Primjer 4 Example 4
3-ciano-4-(2,2-diklorociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-(2,2-dichlorocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Benziltrietilamonij klorid (0,01 g) i etanol (0,015 ml) dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 4 (0,46 g) u kloroformu (0,66 ml). Zatim je dodana 50 % vodena otopina natrij hidroksida (0,25 ml) i reakcijska smjesa je mijeÅ”ana na 60 Ā°C tokom 1 mjeseca. RezultirajuÄa smjesa je podijeljena izmeÄu diklorometana i vode, zatim je organska faza izdvojena, osuÅ”ena (MgSO4) i isparena pod sniženim tlakom. SmeÄa guma tako dobivena je proÄiÅ”Äena kromatografijom stupca na silikagelu (10 g), koristeÄi diklorometan kao eluant, praÄeno obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (50:40:10) kao eluanta. Kristalizacija zahtjevanog materijala iz heksana dala je spoj iz naslova kao bezbojne ploÄice, t.t. 123-126 Ā°C. Benzyltriethylammonium chloride (0.01 g) and ethanol (0.015 ml) were added to a stirred solution of the title compound of Preparation 4 (0.46 g) in chloroform (0.66 ml). A 50% aqueous solution of sodium hydroxide (0.25 ml) was then added and the reaction mixture was stirred at 60 Ā°C for 1 month. The resulting mixture was partitioned between dichloromethane and water, then the organic phase was separated, dried (MgSO4) and evaporated under reduced pressure. The brown gum thus obtained was purified by column chromatography on silica gel (10 g), using dichloromethane as eluent, followed by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (50:40:10) as eluent. Crystallization of the required material from hexane gave the title compound as colorless plates, m.p. 123-126 Ā°C.
Ī“ (CDCl3): 1,84 (t, 1H); 2,20 (dd, 1H); 2,85 (dd, 1H); 7,53 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 1.84 (t, 1H); 2.20 (dd, 1H); 2.85 (dd, 1H); 7.53 (s, 1H); 7.78 (s, 2H).
MS (termosprej): M/Z [M+NH4] 430,6. MS (thermospray): M/Z [M+NH4] 430.6.
C14H6Cl4F3N3 +NH4 zahtijeva 430,96. C14H6Cl4F3N3 +NH4 requires 430.96.
Primjer 5 Example 5
5-amino-3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-pentafluorotiofenil)pirazol 5-amino-3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole
Bromoform (6,4 ml), praÄen etanolom (0,1 ml) i otopinom natrij hidroksida (0,29 g) u vodi (0,5 ml), dodani su u izmijeÅ”anu otopinu spoja iz naslova iz pripreme 6 (0,35 g) u diklorometanu (2 ml). Benziltrietilamonij klorid (0,01 g) je zatim dodan i reakcijska smjesa je mijeÅ”ana na 50 Ā°C tokom 13 dana, zatim je ostavljena da se ohladi. RezultirajuÄa smjesa je isparena pod sniženim tlakom i ostatak je podijeljen izmeÄu diklorometana i vode. Organska faza je izdvojena i kombinirana sa ekstraktima etil acetata iz vodene faze, zatim su kombinirane organske otopine isprane sa slanom vodom, osuÅ”ene i isparene pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi diklorometan kao eluant, praÄeno obrnutom fazom HPLC na C18 silikagelu, koristeÄi acetonitril:voda:metanol (60:30:10) kao eluanta, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 178-180 Ā°C. Bromoform (6.4 ml), followed by ethanol (0.1 ml) and a solution of sodium hydroxide (0.29 g) in water (0.5 ml) were added to a mixed solution of the title compound from Preparation 6 (0.35 g) in dichloromethane (2 ml). Benzyltriethylammonium chloride (0.01 g) was then added and the reaction mixture was stirred at 50 Ā°C for 13 days, then allowed to cool. The resulting mixture was evaporated under reduced pressure and the residue partitioned between dichloromethane and water. The organic phase was separated and combined with ethyl acetate extracts from the aqueous phase, then the combined organic solutions were washed with salt water, dried and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using dichloromethane as eluent, followed by reverse phase HPLC on C18 silica gel, using acetonitrile:water:methanol (60:30:10) as eluent, to afford the title compound as a white solid, m.p. 178-180 Ā°C.
Ī“ (CDCl3): 2,29 (d, 2H); 2,60 (t, 1H); 3,89 (br.s, 2H); 7,93 (d, 2H). Ī“ (CDCl 3 ): 2.29 (d, 2H); 2.60 (t, 1H); 3.89 (no.s, 2H); 7.93 (d, 2H).
MS (termosprej): M/Z [M+H] 574,7. MS (thermospray): M/Z [M+H] 574.7.
C13H7Br2Cl2F5N4S+H zahtijeva 574,81. C13H7Br2Cl2F5N4S+H requires 574.81.
Primjer 6 Example 6
3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-pentafluorotiofenil)pirazol 3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole
Dobiven je kao bijela pjena iz spoja iz naslova pripreme 8 analogno sa primjerom 5, ali koristeÄi heksan:diklorometan (1:1) kao eluanta u poÄetnoj fazi proÄiÅ”Äavanja kromatografije stupca. It was obtained as a white foam from the title compound of preparation 8 analogously to example 5, but using hexane:dichloromethane (1:1) as eluent in the initial stage of column chromatography purification.
Ī“ (CDCl3): 2,01 (t, 1H); 2,34 (dd, 1H); 2,88 (dd, 1H); 7,54 (s, 1H); 7,91 (d, 2H). Ī“ (CDCl 3 ): 2.01 (t, 1H); 2.34 (dd, 1H); 2.88 (dd, 1H); 7.54 (s, 1H); 7.91 (d, 2H).
MS (termosprej) M/Z [M+NH4] 576,8. MS (thermospray) M/Z [M+NH4] 576.8.
C13H6Br2Cl2F5N3S+NH4 zahtijeva 576,83. C13H6Br2Cl2F5N3S+NH4 requires 576.83.
Primjer 7 Example 7
3-ciano-4-ciklopropil-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-cyclopropyl-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
0,2 M otopine diazometana u eteru (25 ml) dodano je tokom 25 minuta u izmijeÅ”anu otopinu spoja iz naslova pripreme 4 (0,332 g) i paladij(II) acetata (0,02 g) u eter (10 ml) i smjesa je mijeÅ”ana na sobnoj temperaturi tokom 18 sati. Reakcijska smjesa je tretirana sa dodatnim koliÄinama eterske otopine diazometana (25 ml) i paladij(II) acetata (0,01 g), mijeÅ”ana je tokom 24 sata, dalje je tretirana sa eterskom otopinom diazometana (50 ml) i paladij(II) acetata (0,01 g), mijeÅ”ana joÅ” 24 sata, zatim je isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (5 g), koristeÄi diklorometan kao eluanta, praÄeno obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (50:45:5) kao eluanta, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 124 Ā°C. A 0.2 M solution of diazomethane in ether (25 ml) was added over 25 minutes to a mixed solution of the compound from the title preparation 4 (0.332 g) and palladium(II) acetate (0.02 g) in ether (10 ml) and the mixture was stirred at room temperature for 18 hours. The reaction mixture was treated with additional amounts of ethereal solution of diazomethane (25 ml) and palladium(II) acetate (0.01 g), stirred for 24 hours, further treated with ethereal solution of diazomethane (50 ml) and palladium(II) acetate (0.01 g), stirred for another 24 hours, then evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (5 g), using dichloromethane as eluent, followed by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (50:45:5) as eluent, to give the title compound as a white solid product, m.p. 124 Ā°C.
Ī“ (CDCl3): 0,77 (m, 2H); 1,07 (m, 2H); 1,89 (m, 1H); 7,29 (s, 1H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 0.77 (m, 2H); 1.07 (m, 2H); 1.89 (m, 1H); 7.29 (s, 1H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+NH4] 362,8. MS (thermospray): M/Z [M+NH 4 ] 362.8.
C14 H8 Cl2 F3 N3 +NH4 zahtijeva 363,04. C14 H8 Cl2 F3 N3 +NH4 requires 363.04.
Primjer 8 Example 8
3-ciano-4-(2,2-dibromo-3,3-dimetilciklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-(2,2-dibromo-3,3-dimethylcyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Otopina spoja iz naslova pripreme 10 (0,15 g) i feniltribromometil-živa (0,44 g) u toluenu (2 ml) zagrijavana je na 70 Ā°C tokom 5 sati, ostavljena je da se ohladi i isparena je pod sniženim tlakom. Ostatak je proÄiÅ”Äen obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (60:30:10) kao eluanta, radi dobivanja spoja iz naslova kao sasvim bijeli Ävrsti proizvod, t.t. 146-148 Ā°C. A solution of the title compound of preparation 10 (0.15 g) and phenyltribromomethylmercury (0.44 g) in toluene (2 ml) was heated at 70 Ā°C for 5 hours, allowed to cool and evaporated under reduced pressure. The residue was purified by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (60:30:10) as eluent, to give the title compound as an off-white solid, m.p. 146-148 Ā°C.
Ī“ (CDCl3): 1,31 (s, 3H); 1,70 (s, 3H); 2,52 (s, 1H); 7,78 (s, 2H); 7,79 (s, 1H). Ī“ (CDCl 3 ): 1.31 (s, 3H); 1.70 (s, 3H); 2.52 (s, 1H); 7.78 (s, 2H); 7.79 (s, 1H).
MS (termosprej): M/Z [M+NH4] 546,7. MS (thermospray): M/Z [M+NH 4 ] 546.7.
C16H10Br2Cl2F3N3 +NH4 zahtijeva 546,89. C16H10Br2Cl2F3N3 +NH4 requires 546.89.
Primjer 9 Example 9
3-ciano-4-(2,2-dibromo-1-metilciklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-(2,2-dibromo-1-methylcyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Dobiven je iz spoja iz naslova pripreme 15 analogno sa primjerom 8, ali koriÅ”tenjem reakcijskog vremena od 4 sata praÄeno filtracijom reakcijske smjese i poÄetnom fazom proÄiÅ”Äavanja kromatografijom stupca na silikagelu koristeÄi heksan:diklorometan (1:1) kao eluanta, kao bijeli Ävrsti proizvod, t.t. 133-134 Ā°C. It was obtained from the compound from the title of preparation 15 analogously to example 8, but using a reaction time of 4 hours followed by filtration of the reaction mixture and an initial stage of purification by column chromatography on silica gel using hexane:dichloromethane (1:1) as eluent, as a white solid product, m.p. 133-134 Ā°C.
Ī“ (CDCl3): 1,83 (s, 3H); 1,92 (d, 1H); 2,28 (d, 1H); 7,59 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 1.83 (s, 3H); 1.92 (d, 1H); 2.28 (d, 1H); 7.59 (s, 1H); 7.78 (s, 2H).
MS (termosprej): M/Z [M+NH4] 533,0. MS (thermospray): M/Z [M+NH 4 ] 533.0.
C15 H8 Br2 Cl2 F3 N3 +NH4 zahtijeva 532,88. C15 H8 Br2 Cl2 F3 N3 +NH4 requires 532.88.
Primjer 10 Example 10
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(1-metilciklopropil)-pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-methylcyclopropyl)-pyrazole
0,007 M otopine diazometana u eteru (20 ml) dodano je u 2 jednaka dijela u izmijeÅ”anu otopinu spoja iz naslova pripreme 15 (0,346 g) i paladij(II) acetata (0,01 g) u eteru (10 ml) i smjesa je mijeÅ”ana na sobnoj temperaturi tokom 48 sati, zatim je filtrirana. Reakcijska smjesa je tretirana sa dodatnim koliÄinama eterske otopine diazometana (20 ml) i paladij(II) acetata (0,01 g), mijeÅ”ana je tokom 24 sata i filtrirana, zatim je ovaj ciklus ponovljen. Reakcijska smjesa je dalje tretirana sa eterskom otopinom diazometana (20 ml) i paladij(II) acetatom (0,01 g), mijeÅ”ana je tokom 5 dana, filtrirana i isparena pod sniženim tlakom. Kristalizacija ostatka iz cikloheksana dala je spoj iz naslova kao žuti Ävrsti proizvod, t.t. 138-139 Ā°C. A 0.007 M solution of diazomethane in ether (20 ml) was added in 2 equal portions to a mixed solution of the title compound 15 (0.346 g) and palladium(II) acetate (0.01 g) in ether (10 ml) and the mixture was stirred at room temperature for 48 hours, then filtered. The reaction mixture was treated with additional amounts of ether solution of diazomethane (20 ml) and palladium(II) acetate (0.01 g), stirred for 24 hours and filtered, then this cycle was repeated. The reaction mixture was further treated with an ethereal solution of diazomethane (20 ml) and palladium(II) acetate (0.01 g), stirred for 5 days, filtered and evaporated under reduced pressure. Crystallization of the residue from cyclohexane gave the title compound as a yellow solid, m.p. 138-139 Ā°C.
Ī“ (CDCl3): 0,86 (m, 2H); 1,04 (m, 2H); 1,50 (s, 3H); 7,41 (s, 1H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 0.86 (m, 2H); 1.04 (m, 2H); 1.50 (s, 3H); 7.41 (s, 1H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+H] 359,8. MS (thermospray): M/Z [M+H] 359.8.
C15H10Cl2F3N3 +H zahtijeva 360,03. C15H10Cl2F3N3 +H requires 360.03.
Primjer 11 Example 11
3-ciano-4-(2,2-dibromo-1-metoksiciklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-(2,2-dibromo-1-methoxycyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Otopina spoja iz naslova pripreme 17 (0,4 g) i feniltribromometil-živa (0,76 g) u toluenu (1 ml) zagrijavana je na 60 Ā°C tokom 4 sata, ostavljena je da se ohladi i isparena je pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:dihlorometan (1:1) kao eluanta, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 117-118 Ā°C. A solution of the title compound 17 (0.4 g) and phenyltribromomethylmercury (0.76 g) in toluene (1 ml) was heated at 60 Ā°C for 4 hours, allowed to cool and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using hexane:dichloromethane (1:1) as eluent, to give the title compound as a white solid, m.p. 117-118 Ā°C.
Ī“ (CDCl3): 2,22 (d, 1H); 2,40 (d, 1H); 3,43 (s, 3H); 7,80 (s, 2H); 7,84 (s, 1H). Ī“ (CDCl 3 ): 2.22 (d, 1H); 2.40 (d, 1H); 3.43 (s, 3H); 7.80 (s, 2H); 7.84 (s, 1H).
MS (termosprej): M/Z [M+H] 532,1. MS (thermospray): M/Z [M+H] 532.1.
C15H8Br2CL2F3N3O+H zahtijeva 531,84. C15H8Br2CL2F3N3O+H requires 531.84.
Primjer 12 Example 12
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(2,2,3,3-tetrametilciklopropil)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(2,2,3,3-tetramethylcyclopropyl)pyrazole
Otopina spoja iz naslova pripreme 18 (0,04 g), 2,3-dimetilbut-2-ena (1,08 ml) i rodij(II) acetat dimer (0,001 g) u diklorometanu (0,3 ml) zagrijavano je na 70 Ā°C tokom 30 minuta i držano je na ovoj temperaturi daljnjih 30 minuta. Diklorometan (0,3 ml) je dodan u reakcijsku smjesu koja je zatim zagrijavana tokom slijedeÄeg 1 sata, ostavljena je da se ohladi i podijeljena je izmeÄu diklorometana (5 ml) i vode (2 ml). Organska faza je izdvojena, osuÅ”ena(NA2SO4) i isparena pod sniženim tlakom, zatim je ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu (1 g), koristeÄi diklorometan kao eluanta, radi dobivanja spoja iz naslova kao bijeli Ävrsti kristalni proizvod, t.t. 158-159 Ā°C. A solution of the title compound 18 (0.04 g), 2,3-dimethylbut-2-ene (1.08 ml) and rhodium(II) acetate dimer (0.001 g) in dichloromethane (0.3 ml) was heated at 70 Ā°C for 30 minutes and held at this temperature for a further 30 minutes. Dichloromethane (0.3 ml) was added to the reaction mixture which was then heated for the next 1 hour, allowed to cool and partitioned between dichloromethane (5 ml) and water (2 ml). The organic phase was separated, dried (NA2SO4) and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel (1 g), using dichloromethane as eluent, to obtain the title compound as a white solid crystalline product, m.p. 158-159 Ā°C.
Ī“ (CDCl3): 1,05 (s, 6H); 1,33 (s, 6H); 1,55 (s, 1H); 7,38 (s, 1H); 7,75 (s, 2H). Ī“ (CDCl 3 ): 1.05 (s, 6H); 1.33 (s, 6H); 1.55 (s, 1H); 7.38 (s, 1H); 7.75 (s, 2H).
MS (termosprej): M/Z [M+NH4] 419,6. MS (thermospray): M/Z [M+NH 4 ] 419.6.
C18H16Cl2F3N3 +NH4 zahtijeva 419,1. C18H16Cl2F3N3 +NH4 requires 419.1.
Primjer 13 Example 13
3-ciano-4-(t-2,t-3-dikloro-r-1-ciklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-(t-2,t-3-dichloro-r-1-cyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Otopina spoja iz naslova pripreme 18 (0,254 g), cis-1,2-dikloroetilen (7,0 g) i rodij(II) acetat dimer (0,045 g) u nevodenom diklorometanu (7,5 ml) zagrijavana je na 60 Ā°C tokom 4,5 sata i zatim je ostavljena da stoji na sobnoj temperaturi tokom 18 sati. RezultirajuÄa smjesa je proÄiÅ”Äena kromatografijom stupca na silikagelu (50 g), koristeÄi diklorometan kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 138-139 Ā°C. A solution of the title compound 18 (0.254 g), cis-1,2-dichloroethylene (7.0 g) and rhodium(II) acetate dimer (0.045 g) in anhydrous dichloromethane (7.5 ml) was heated to 60 Ā°C for 4.5 hours and then left to stand at room temperature for 18 hours. The resulting mixture was purified by column chromatography on silica gel (50 g), using dichloromethane as eluent, to afford the title compound as a white solid, m.p. 138-139 Ā°C.
Ī“ (CDCl3): 2,80 (t, 1H); 3,80 (d, 2H); 7,75 (s, 1H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 2.80 (t, 1H); 3.80 (d, 2H); 7.75 (s, 1H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+NH4] 431,1. MS (thermospray): M/Z [M+NH4] 431.1.
C14H6Cl4F3N3 +NH4 zahtijeva 430,96. C14H6Cl4F3N3 +NH4 requires 430.96.
Primjer 14 Example 14
3-ciano-4-(t-2,t-3-dibromo-r-1-ciklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-(t-2,t-3-dibromo-r-1-cyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Dobiven je iz spoja iz naslova pripreme 18 i 1,2-dibromoetilena analogno sa primjerom 13, ali zagrijavanje reakcijske smjese na 55 Ā°C tokom 4 sata i konaÄno suÅ”enje zaleÄivanjem ostatka dalo je nakon faze kromatografskog proÄiÅ”Äavanja iz t-butanola, blijedo žuti Ävrsti proizvod, t.t. 106-108 Ā°C. It was obtained from the title compound of the preparation 18 and 1,2-dibromoethylene analogously to example 13, but heating the reaction mixture at 55 Ā°C for 4 hours and finally freeze-drying the residue gave, after a step of chromatographic purification from t-butanol, a pale yellow solid product , m.p. 106-108 Ā°C.
Ī“ (CDCl3): 2,76 (t, 1H); 3,80 (d, 2H); 7,78 (s, 2H); 7,80 (s, 1H). Ī“ (CDCl 3 ): 2.76 (t, 1H); 3.80 (d, 2H); 7.78 (s, 2H); 7.80 (s, 1H).
MS (termosprej): M/Z [M+H] 502,0. MS (thermospray): M/Z [M+H] 502.0.
C14H6Br2Cl4F3N3 +H zahtijeva 501,83. C14H6Br2Cl4F3N3 +H requires 501.83.
Primjer 15 Example 15
3-ciano-4-(biciklo[3,1,0]heksan-6-il)-1-(2,6-dikloro-4-trifluoro-metilfenil)pirazol 3-cyano-4-(bicyclo[3,1,0]hexan-6-yl)-1-(2,6-dichloro-4-trifluoro-methylphenyl)pyrazole
Dobiven iz spoja iz naslova pripreme 18 i ciklopentena analogno sa primjerom 13, ali zagrijavanjem reakcijske smjese na 55 Ā°C tokom 4 sata, kao bijeli Ävrsti proizvod, t.t. 105-106 Ā°C. Obtained from the title compound of preparation 18 and cyclopentene analogously to example 13, but by heating the reaction mixture at 55 Ā°C for 4 hours, as a white solid product, m.p. 105-106 Ā°C.
Ī“ (CDCl3): 1,41-2,06 (m, 9H); 7,47 (s, 1H); 7,75 (s, 2H). Ī“ (CDCl 3 ): 1.41-2.06 (m, 9H); 7.47 (s, 1H); 7.75 (s, 2H).
MS (termosprej): M/Z [M+NH4] 403,4. MS (thermospray): M/Z [M+NH 4 ] 403.4.
C17 H12 Cl2 F3 N3 + NH4 zahtijeva 403,07. C17 H12 Cl2 F3 N3 + NH4 requires 403.07.
Primjer 16 Example 16
3-ciano-4-(biciklo[4,1,0]heptan-7-il)-1-(2,6-dikloro-4-trifluoro-metilfenil)pirazol 3-cyano-4-(bicyclo[4,1,0]heptan-7-yl)-1-(2,6-dichloro-4-trifluoro-methylphenyl)pyrazole
Dobiven iz spoja iz naslova pripreme 18 i cikloheksena analogno sa primjerom 15, kao bijeli Ävrsti proizvod, t.t. 113-114 Ā°C. Obtained from the title compound of preparation 18 and cyclohexene analogously to example 15, as a white solid product, m.p. 113-114 Ā°C.
Ī“ (CDCL3): 0,87 (m, 2H); 1,21 (m, 2H); 1,46 (m, 2H); 1,59 (m, 2H); 1,78 (t, 1H); 2,04 (m, 2H); 7,52 (s, 1H); 7,77 (s, 2H). Ī“ (CDCl 3 ): 0.87 (m, 2H); 1.21 (m, 2H); 1.46 (m, 2H); 1.59 (m, 2H); 1.78 (t, 1H); 2.04 (m, 2H); 7.52 (s, 1H); 7.77 (s, 2H).
MS (termosprej): M/Z [M+NH4] 417,0. MS (thermospray): M/Z [M+NH 4 ] 417.0.
C18H14Cl2F3N3 + NH4 zahtijeva 417,09. C18H14Cl2F3N3 + NH4 requires 417.09.
Primjer 17 Example 17
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(2,2-dimetil-ciklopropil)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(2,2-dimethyl-cyclopropyl)pyrazole
Otopina spoja iz naslova pripreme 18 (0,507 g) i rodij(II) acetat dimer (0,45 g) u nevodenom diklorometanu (7 ml) postavljena je posudu prekrivenu staklom (50 ml kapaciteta) koja je zatim prelivena dva puta sa duÅ”ikom. Reakcijska posuda je zatim Å”aržirana sa 2-metilpropenom i reakcijska smjesa je zagrijavana na 55 Ā°C tokom 2 sata, zatim je ostavljena da stoji na sobnoj temperaturi tokom 18 sati. RezultirajuÄa smjesa je proÄiÅ”Äena kromatografijom stupca na silikagelu (50 g), koristeÄi diklorometan kao eluant, radi dobivanja spoja iz naslova kao vrlo blijedo žuti Ävrsti proizvod, t.t. 122-123 Ā°C. A solution of the title compound 18 (0.507 g) and rhodium(II) acetate dimer (0.45 g) in anhydrous dichloromethane (7 ml) was placed in a glass-covered vessel (50 ml capacity) which was then flushed twice with nitrogen. The reaction vessel was then charged with 2-methylpropene and the reaction mixture was heated to 55Ā°C for 2 hours, then allowed to stand at room temperature for 18 hours. The resulting mixture was purified by column chromatography on silica gel (50 g), using dichloromethane as eluent, to afford the title compound as a very pale yellow solid, m.p. 122-123 Ā°C.
Ī“ (CDCl3): 0,70 (m, 1H); 0,96 (s, 3H); 1,00 (m, 1H); 1,26 (s, 3H); 1,74 (m, 1H); 7,25 (s, 1H); 7,76 (s, 2H). Ī“ (CDCl 3 ): 0.70 (m, 1H); 0.96 (s, 3H); 1.00 (m, 1H); 1.26 (s, 3H); 1.74 (m, 1H); 7.25 (s, 1H); 7.76 (s, 2H).
MS (termosprej): M/Z [M+NH4] 390,7. MS (thermospray): M/Z [M+NH 4 ] 390.7.
C16H12Cl2F3N3 +NH4 zahtijeva 391,07. C16H12Cl2F3N3 +NH4 requires 391.07.
Primjer 18 Example 18
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(spiro[2,4]heptan-1-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(spiro[2,4]heptan-1-yl)pyrazole
Dobiven iz spoja iz naslova pripreme 18 i metilenciklopentena analogno sa primjerom 15, ali zagrijavanjem reakcijske smjese tokom samo3 sata, kao blijedo žuti Ävrsti proizvod, t.t. 117-118 Ā°C. Obtained from the compound from the title preparation 18 and methylenecyclopentene analogously to example 15, but by heating the reaction mixture for only 3 hours, as a pale yellow solid product, m.p. 117-118 Ā°C.
Ī“ (CDCl3): 0,88 (t, 1H); 1,22 (dd, 1H); 1,37 (m, 2H); 1,74 (m, 6H); 1,92 (dd, 1H); 7,27 (s, 1H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 0.88 (t, 1H); 1.22 (dd, 1H); 1.37 (m, 2H); 1.74 (m, 6H); 1.92 (dd, 1H); 7.27 (s, 1H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+NH4] 417,1. MS (thermospray): M/Z [M+NH 4 ] 417.1.
C18H14Cl2F3N3 +NH4 zahtijeva 417,09. C18H14Cl2F3N3 +NH4 requires 417.09.
Primjer 19 Example 19
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(2,2-difluoro-ciklopropil)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(2,2-difluoro-cyclopropyl)pyrazole
Dobiven iz spoja iz naslova pripreme 18 i 1,1-difluoroetilena analogno sa primjerom 17, ali zagrijavajuÄi reakcijsku smjesu na 50 Ā°C i pri 2068 kPa (300 psi) tokom 24 sata. Proizvod je dalje proÄiÅ”Äen sa ponovljenom obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda (55:45) kao eluant, za dobivanje spoja iz naslova kao bijeli bezobliÄni Ävrsti proizvod. Obtained from the title compound Preparation of 18 and 1,1-difluoroethylene analogously to Example 17, but heating the reaction mixture to 50 Ā°C and at 2068 kPa (300 psi) for 24 hours. The product was further purified with repeated reverse phase HPLC on C18 silica, using acetonitrile:water (55:45) as eluent, to afford the title compound as a white amorphous solid.
Ī“ (CDCl3): 1,58 (m, 1H); 2,16 (m, 1H); 2,76 (m, 1H); 7,50 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 1.58 (m, 1H); 2.16 (m, 1H); 2.76 (m, 1H); 7.50 (s, 1H); 7.78 (s, 2H).
MS (APCI): M/Z [M+H] 382,0. MS (APCI): M/Z [M+H] 382.0.
C14H6Cl2F5N3 +H zahtijeva 381,99. C14H6Cl2F5N3 +H requires 381.99.
Primjer 20 Example 20
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(spiro[2,3]heksan-1-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(spiro[2,3]hexan-1-yl)pyrazole
Dobiven iz spoja iz naslova pripreme 18 i metilenciklobutana analogno sa primjerom 15, ali zagrijavajuÄi reakcijsku smjesu pod refluksom tokom 4 sata i zatim je ispuÅ”teno slijedeÄe stajanje preko noÄi na sobnoj temperaturi, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 108-110 Ā°C. Obtained from the title compound of the preparation 18 and methylenecyclobutane analogously to Example 15, but heating the reaction mixture under reflux for 4 hours and then omitting the following overnight stand at room temperature, to obtain the title compound as a white solid product, m.p. 108-110 Ā°C.
Ī“ (CDCl3): 0,79 (m, 1H); 1,24 (m, 1H); 1,86-2,39 (m, 7H); 7,08 (s, 1H); 7,76 (s, 2H). Ī“ (CDCl 3 ): 0.79 (m, 1H); 1.24 (m, 1H); 1.86-2.39 (m, 7H); 7.08 (s, 1H); 7.76 (s, 2H).
MS (termosprej); M/Z [M+NH4] 403,0. MS (thermospray); M/Z [M+NH 4 ] 403.0.
C17H12Cl2F3N3 +NH4 zahtijeva 403,07. C17H12Cl2F3N3 +NH4 requires 403.07.
Primjer 21 Example 21
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(spiro[2,2]pentan-2-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(spiro[2,2]pentan-2-yl)pyrazole
IzmijeÅ”ana otopina spoja iz naslova pripreme 18 (0,507 g), metilenciklopropana (5 ml) i rodij(II) acetat dimer (0,045 g) u nevodenom diklorometanu (7 ml) zagrijavana je na 55 Ā°C tokom 24 sata u zatvorenom, debelo obloženom, staklenom kontejneru i zatim je ostavljena da se ohladi. RezultirajuÄa smjesa je proÄiÅ”Äena kao u primjeru 13 radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 108-110 Ā°C. A mixed solution of the title compound 18 (0.507 g), methylenecyclopropane (5 ml) and rhodium(II) acetate dimer (0.045 g) in anhydrous dichloromethane (7 ml) was heated to 55 Ā°C for 24 hours in a closed, thickly lined, glass container and then left to cool. The resulting mixture was purified as in Example 13 to give the title compound as a white solid, m.p. 108-110 Ā°C.
Ī“ (CDCl3): 0,81 (m, 1H); 0,91 (m, 1H); 0,99-1,18 (m, 3H); 1,66 (dd, 1H); 2,21 (dd, 1H); 7,29 (s, 1H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 0.81 (m, 1H); 0.91 (m, 1H); 0.99-1.18 (m, 3H); 1.66 (dd, 1H); 2.21 (dd, 1H); 7.29 (s, 1H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+NH4] 389,1. MS (thermospray): M/Z [M+NH 4 ] 389.1.
C16H10Cl2F3N3 +NH4 zahtijeva 389,05 C16H10Cl2F3N3 +NH4 requires 389.05
Primjer 22 Example 22
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-metilpirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-methylpyrazole
Bromoform (1,08 m), praÄeno otopinom natrij hidroksida (0,495 g) u vodi (1 ml) i etanolu (0,1 ml), dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 22 (0,993 g) u diklorometanu (4 ml). Benziltrietilamonij klorid (0,222 g) dodan je zatim i reakcijska smjesa je zagrijavana na 50 Ā°C tokom 6 dana. Iste koliÄine bromoforma, vodene otopine natrij hidroksida i etanola opet su dodane i mijeÅ”anje na 50 Ā°C je nastavljeno tokom 5 dana. Hladna reakcijska smjesa je podijeljena izmeÄu etera i vode, zatim je vodena faza izdvojena i ekstrahirana sa eterom (Ć 2). Kombinirane organske otopine su osuÅ”ene (Na2SO4) i isparene pod sniženim tlakom, zatim je ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:diklorometan (3:2) kao eluanta, praÄeno trituracijom sa hladnim heksanom, radi dobivanja spoja iz naslova kao sasvim bijeli Ävrsti proizvod, t.t. 66,8-68,2 Ā°C. Bromoform (1.08 g), followed by a solution of sodium hydroxide (0.495 g) in water (1 ml) and ethanol (0.1 ml), were added to a stirred solution of the title compound 22 (0.993 g) in dichloromethane (4 ml ). Benzyltriethylammonium chloride (0.222 g) was then added and the reaction mixture was heated at 50 Ā°C for 6 days. The same amounts of bromoform, aqueous sodium hydroxide and ethanol were added again and stirring at 50 Ā°C was continued for 5 days. The cold reaction mixture was partitioned between ether and water, then the aqueous phase was separated and extracted with ether (Ć2). The combined organic solutions were dried (Na2SO4) and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel, using hexane:dichloromethane (3:2) as eluent, followed by trituration with cold hexane, to give the title compound as an off-white solid product, m.p. 66.8-68.2 Ā°C.
Ī“ (CDCl3): 1,87 (t, 1H); 2,19 (dd, 1H); 2,47 (s, 3H); 2,64 (dd, 1H); 7,22 (s, 1H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 1.87 (t, 1H); 2.19 (dd, 1H); 2.47 (s, 3H); 2.64 (dd, 1H); 7.22 (s, 1H); 7.80 (s, 2H).
MS (termosprej) M/Z [M+H] 491,0. MS (thermospray) M/Z [M+H] 491.0.
C14H9Br2Cl2F3N2 +H zahtijeva 490,85. C14H9Br2Cl2F3N2 +H requires 490.85.
Primjer 23 Example 23
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3,5-dimetilpirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3,5-dimethylpyrazole
Bromoform (1,1 g), praÄeno otopinom natrij hidroksida (0,175 g) u vodi (0,5 ml) i etanolu (0,1 ml), dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 25 (0,368 g) u diklorometanu (2 ml). Benziltrietilamonij klorid (0,01 g) dodan je zatim i reakcijska smjesa je zagrijavana na refluksu tokom 4 dana. Iste koliÄine bromoforma, vodene otopine natrij hidroksida i etanola opet su dodane i mijeÅ”anje je nastavljeno pod refluksom tokom 9 dana. Hladna reakcijska smjesa je razblažena sa diklorometanom (20 ml), zatim je ova smjesa isprana sukcesivno sa vodom (3 Ć 15 ml) i slanom vodom (10 ml), osuÅ”ena (MgSO4) i isparena pod tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (30 g) koristeÄi heksan i zatim heksan:eter:diklorometan (8:1:1) kao eluante, praÄeno obrnutom fazom HPLC na C18 silicij dioksidu koristeÄi acetonitril:voda:metanol (60:30:10) kao eluant, radi dobivanja spoja iz naslova kao ulje. Bromoform (1.1 g), followed by a solution of sodium hydroxide (0.175 g) in water (0.5 ml) and ethanol (0.1 ml), were added to a stirred solution of the title compound 25 (0.368 g) in dichloromethane ( 2 ml). Benzyltriethylammonium chloride (0.01 g) was then added and the reaction mixture was heated at reflux for 4 days. The same amounts of bromoform, aqueous sodium hydroxide and ethanol were added again and stirring was continued under reflux for 9 days. The cold reaction mixture was diluted with dichloromethane (20 ml), then this mixture was washed successively with water (3 x 15 ml) and brine (10 ml), dried (MgSO4) and evaporated under pressure. The residue was purified by column chromatography on silica gel (30 g) using hexane and then hexane:ether:dichloromethane (8:1:1) as eluants, followed by reverse phase HPLC on C18 silica using acetonitrile:water:methanol (60:30:10 ) as eluent, to obtain the title compound as an oil.
Ī“ (CDCl3): 1,93 (t, 1H); 2,10 (2, 3H); 2,19 (dd, 1H); 2,36 (s, 3H); 2,60 (dd, 1H); 7,73 (s, 2H). Ī“ (CDCl 3 ): 1.93 (t, 1H); 2.10 (2.3H); 2.19 (dd, 1H); 2.36 (s, 3H); 2.60 (dd, 1H); 7.73 (s, 2H).
MS (termosprej): M/Z [M+H] 504,9. MS (thermospray): M/Z [M+H] 504.9.
C15H11Br2Cl2F3N2 +H zahtijeva 504,87. C15H11Br2Cl2F3N2 +H requires 504.87.
Primjer 24 Example 24
4-(2,2-dibromociklopropil)-3-metil-1-(2,4,6-triklorofenil)pirazol 4-(2,2-dibromocyclopropyl)-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole
Otopina natrij hidroksida (0,64 g) u vodi (1 ml) i etanolu (0,1 ml) dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 28 (1,0 g), bromoforma (2 ml) i benziltrietilamonij klorida (0,04 g) u diklorometanu (2 ml) i reakcijska smjesa je zagrijavana pod refluksom tokom 16 sati, zatim je ostavljena da se ohladi. RezultirajuÄa smjesa je podijeljena izmeÄu diklorometana i vode, zatim je organska faza izdvojena, isprana sukcesivno sa vodom i slanom vodom, osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:etil acetat (50:1) kao eluant, radi dobivanja žutog ulja koje je dalje proÄiÅ”Äeno na sliÄan naÄin, koristeÄi heksan:etil acetat (19:1) kao eluant, praÄeno trituracijom sa propan-2-olom, radi dobivanja spoja iz naslova kao žuti Ävrsti proizvod, t.t. 84-86 Ā°C. A solution of sodium hydroxide (0.64 g) in water (1 ml) and ethanol (0.1 ml) was added to a mixed solution of the title compound 28 (1.0 g), bromoform (2 ml) and benzyltriethylammonium chloride (0 .04 g) in dichloromethane (2 ml) and the reaction mixture was heated under reflux for 16 hours, then allowed to cool. The resulting mixture was partitioned between dichloromethane and water, then the organic phase was separated, washed successively with water and brine, dried (Na2SO4) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using hexane:ethyl acetate (50:1) as eluent, to give a yellow oil which was further purified in a similar manner, using hexane:ethyl acetate (19:1) as eluent, followed by trituration with propane -2-olom, to obtain the title compound as a yellow solid, m.p. 84-86 Ā°C.
Ī“ (CDCl3): 1,79 (t, 1H); 2,19 (dd, 1H); 2,44 (s, 3H); 2,63 (dd, 1H); 7,18 (s, 1H); 7,44 (s, 2H). Ī“ (CDCl 3 ): 1.79 (t, 1H); 2.19 (dd, 1H); 2.44 (s, 3H); 2.63 (dd, 1H); 7.18 (s, 1H); 7.44 (s, 2H).
MS (termosprej): M/Z [M+H] 456,8. MS (thermospray): M/Z [M+H] 456.8.
C13H9Br2Cl3N2 +H zahtijeva 456,83. C13H9Br2Cl3N2 +H requires 456.83.
Primjer 25 Example 25
4-(2,2-diklorociklopropil)-3-metil-1-(2,4,6-triklorofenil)pirazol 4-(2,2-dichlorocyclopropyl)-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole
50 %-na vodena otopina natrij hidroksida (2 ml) dodana je u izmijeÅ”anu otopinu spoja iz naslova pripreme 28 (1,0 g), kloroform (7 ml) i benziltrietilamonij klorid (0,08 g) u smjesu etanola (0,2 ml) i diklorometana (2 ml), zatim je reakcijska smjesa zagrijavana pod refluksom tokom 16 sati. Daljnje koliÄine kloroforma (3 ml), benziltrietilamonij klorida (0,04 g) i otopina natrij hidroksida (1 ml) su dodane, zatim je ova smjesa mijeÅ”ana pod refluksom tokom 16 sati, ostavljena je da se ohladi i podijeljena izmeÄu diklorometana i vode. Organska faza je izdvojena, isprana sukcesivno sa vodom i slanom vodom, osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:etil acetat (19:1) kao eluant, radi dobivanja žutog ulja koje je dalje proÄiÅ”Äeno sa obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (60:30:10) kao eluant, radi dobivanja spoja iz naslova kao bezbojno ulje. A 50% aqueous solution of sodium hydroxide (2 ml) was added to a mixed solution of the compound from the title preparation 28 (1.0 g), chloroform (7 ml) and benzyltriethylammonium chloride (0.08 g) in a mixture of ethanol (0.2 ml) and dichloromethane (2 ml), then the reaction mixture was heated under reflux for 16 hours. Further amounts of chloroform (3 ml), benzyltriethylammonium chloride (0.04 g) and sodium hydroxide solution (1 ml) were added, then this mixture was stirred under reflux for 16 hours, allowed to cool and partitioned between dichloromethane and water. The organic phase was separated, washed successively with water and brine, dried (Na2SO4) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using hexane:ethyl acetate (19:1) as eluent to give a yellow oil which was further purified by reverse phase HPLC on C18 silica using acetonitrile:water:methanol (60:30:10 ) as eluent, to obtain the title compound as a colorless oil.
Ī“ (CDCl3): 1,61 (t, 1H); 2,02 (dd, 1H); 2,42 (s, 3H); 2,63 (dd, 1H); 7,20 (s, 1H); 7,47 (s, 2H). Ī“ (CDCl 3 ): 1.61 (t, 1H); 2.02 (dd, 1H); 2.42 (s, 3H); 2.63 (dd, 1H); 7.20 (s, 1H); 7.47 (s, 2H).
MS (termosprej): M/Z [M+H] 368,8. MS (thermospray): M/Z [M+H] 368.8.
C13H9Cl5N2 +H zahtijeva 368,93. C13H9Cl5N2 +H requires 368.93.
Primjeri 26A i 26B Examples 26A and 26B
A. 4-(c-2-bromo-r-1-ciklopropil)-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol i A. 4-(c-2-bromo-r-1-cyclopropyl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole and
B. 4-(t-2-bromo-r-1-ciklopropil)-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol B. 4-(t-2-bromo-r-1-cyclopropyl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Tri-n-butiltin hidrid (0,9 g) dodan je ukapavanjem, preko Å”trcaljke, u izmijeÅ”anu otopinu spoja iz naslova iz primjera 2 (0,504 g) u toluenu (10 ml) na -10 Ā°C. Reakcijska smjesa je ostavljena da se zagrije na sobnu temperaturu, mijeÅ”ana je tokom 5 sati, držana na -20 Ā°C tokom 3 dana, ponovno ostavljena da se zagrije na sobnu temperaturu i zatim je tretirana sa joÅ” tri-n-butiltin hidrida (0,9 g). Ova smjesa je mijeÅ”ana tokom daljnja 24 sata, tretirana sa vodom i zatim, nakon 30 minuta, vodena faza je izdvojena i ekstrahirana sa diklorometanom. Kombinirane organske faze su osuÅ”ene i isparene pod sniženim tlakom radi dobivanja smeÄeg ulja koje je proÄiÅ”Äeno kromatografijom stupca na silikagelu, koristeÄi heksan:diklorometan (4:1) i zatim diklorometan kao eluanta, praÄeno kristalizacijom zahtjevanog proizvoda iz diprop-2-il etera, radi dobivanja izomera A kao sivkasto-bijeli Ävrsti proizvod, t.t. 120,5-121 Ā°C. Tri-n-butyltin hydride (0.9 g) was added dropwise via syringe to a stirred solution of the title compound from Example 2 (0.504 g) in toluene (10 ml) at -10 Ā°C. The reaction mixture was allowed to warm to room temperature, stirred for 5 hours, kept at -20 Ā°C for 3 days, allowed to warm to room temperature again, and then treated with more tri-n-butyltin hydride (0, 9 g). This mixture was stirred for a further 24 hours, treated with water and then, after 30 minutes, the aqueous phase was separated and extracted with dichloromethane. The combined organic phases were dried and evaporated under reduced pressure to give a brown oil which was purified by column chromatography on silica gel, using hexane:dichloromethane (4:1) and then dichloromethane as eluent, followed by crystallization of the desired product from diprop-2-yl ether, to obtaining isomer A as a grayish-white solid product, m.p. 120.5-121 Ā°C.
Ī“ (CDCl3: 1,22 (m, 1H);1,82 (m, 1H);2,29 (m, 1H);3,40 (m, 1H);7,47 (s, 1H);7,78 (s, 2H). Ī“ (CDCl3: 1.22 (m, 1H); 1.82 (m, 1H); 2.29 (m, 1H); 3.40 (m, 1H); 7.47 (s, 1H); 7 .78 (s, 2H).
MS (termosprej): M/Z [M+NH4] 441,0. C14H7BrCl2F3N3 +NH4 zahtijeva 440,95. MS (thermospray): M/Z [M+NH 4 ] 441.0. C14H7BrCl2F3N3 +NH4 requires 440.95.
ProÄiÅ”Äavanje kristalizacijom matiÄne tekuÄine obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (50:40:10) kao eluanta, dalo je izomer B kao sivkasto-bijeli Ävrsti proizvod, t.t. 126 Ā°C. Purification by crystallization of the mother liquor by reversed-phase HPLC on C18 silica, using acetonitrile:water:methanol (50:40:10) as eluent, gave isomer B as an off-white solid, m.p. 126 Ā°C.
Ī“ (CDCl3): 1,59 (m, 1H); 1,62 (m, 1H); 2,40 (m, 1H); 3,14 (m, 1H); 7,39 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 1.59 (m, 1H); 1.62 (m, 1H); 2.40 (m, 1H); 3.14 (m, 1H); 7.39 (s, 1H); 7.78 (s, 2H).
MS (termosprej): M/Z [M+NH4] 441,4. C14H7BrCl2F3N3 +NH4 zahtijeva 440,95. MS (thermospray): M/Z [M+NH 4 ] 441.4. C14H7BrCl2F3N3 +NH4 requires 440.95.
Primjer 27 Example 27
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(1-trifluorometilciklopropil)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-trifluoromethylcyclopropyl)pyrazole
Otopina spoja iz naslova pripreme 31 (27 g) u ksilenu (250 ml) zagrijavana je pod blagim refluksom tokom 16 sati, zatim je otapalo uklonjeno isparavanjem pod sniženim tlakom. RezultirajuÄi ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (1 kg), koristeÄi heksan i zatim heksan:eter (8:1) kao eluante, praÄeno kristalizacijom iz cikloheksana, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 141 Ā°C. A solution of the compound from the title preparation 31 (27 g) in xylene (250 ml) was heated under gentle reflux for 16 hours, then the solvent was removed by evaporation under reduced pressure. The resulting residue was purified by column chromatography on silica gel (1 kg) using hexane and then hexane:ether (8:1) as eluants, followed by crystallization from cyclohexane to afford the title compound as a white solid, m.p. 141 Ā°C.
Ī“ (CDCl3): 1,24 (m, 2H); 1,52 (m, 2H); 7,72 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 1.24 (m, 2H); 1.52 (m, 2H); 7.72 (s, 1H); 7.78 (s, 2H).
MS (termosprej): M/Z [M+NH4] 431,3. C15H7Cl2F6N3 +NH4 zahtijeva 431,0. MS (thermospray): M/Z [M+NH4] 431.3. C15H7Cl2F6N3 +NH4 requires 431.0.
Primjer 28 Example 28
5-kloro-3-ciano-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 5-chloro-3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
U izmijeÅ”anu otopinu spoja iz naslova od Pripreme 33 (0,288 g) u diklorometanu (1 ml) dodan je bromoform (0,275 ml) praÄeno otopinom natrij hidroksida (0,126 g) u vodi (0,25 ml) i etanola (0,05 ml). Benziltrietilamonij klorid (0,006 g) je zatim dodan i reakcijska smjesa je jako mijeÅ”ana na sobnoj temperaturi tokom 48 sati, zagrijavana na 50Ā°C tokom 7 sati i zatim mijeÅ”ana na sobnoj temperaturi tokom 24 sata. Nakon daljnjeg zagrijavanja na 50Ā°C tokom 24 sata, bromoform (0,275 ml), otopina natrij hidroksida (0,126 g) u vodi (0,25 ml) i etanol (0,05 ml) dodani su i zagrijavanje je nastavljeno tokom 72 sata. Reakcijska smjesa je ohlaÄena, podijeljena izmeÄu etera i vode i vodena faza je izdvojena i ekstrahirana sa eterom (x 2). Kombinirani organski ekstrakti su isprani sa slanom vodom, osuÅ”eni (Na2SO4) i ispareni pod sniženim tlakom, zatim je ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:diklorometan (3:2) kao eluanta, praÄeno kristalizacijom iz heksana, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 103,5-104,2 Ā°C. Bromoform (0.275 ml) was added to a mixed solution of the title compound from Preparation 33 (0.288 g) in dichloromethane (1 ml) followed by a solution of sodium hydroxide (0.126 g) in water (0.25 ml) and ethanol (0.05 ml). . Benzyltriethylammonium chloride (0.006 g) was then added and the reaction mixture was stirred vigorously at room temperature for 48 hours, heated to 50Ā°C for 7 hours and then stirred at room temperature for 24 hours. After further heating at 50Ā°C for 24 hours, bromoform (0.275 ml), a solution of sodium hydroxide (0.126 g) in water (0.25 ml) and ethanol (0.05 ml) were added and heating was continued for 72 hours. The reaction mixture was cooled, partitioned between ether and water, and the aqueous phase was separated and extracted with ether (x 2). The combined organic extracts were washed with brine, dried (Na2SO4) and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel, using hexane:dichloromethane (3:2) as eluent, followed by crystallization from hexane, to give the title compound as a white solid, m.p. 103.5-104.2 Ā°C.
Ī“ (CDCl3): 2,31 (dd, 1H); 2,42 (t, 1H); 2,78 (dd, 1H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 2.31 (dd, 1H); 2.42 (t, 1H); 2.78 (dd, 1H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+NH4] 552,9. C14H5Br2Cl3F3N3 +NH4 zahtijeva 552,82. MS (thermospray): M/Z [M+NH 4 ] 552.9. C14H5Br2Cl3F3N3 +NH4 requires 552.82.
Primjer 29 Example 29
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-trifluorometil)pirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethyl)pyrazole
U izmijeÅ”anu otopinu spoja iz naslova pripreme 36 (0,530 g) u diklorometanu (3 ml) dodan je bromoform (0,49 ml) praÄeno otopinom natrij hidroksida (0,226 g) u vodi (1 ml) i etanola (0,1 ml). Benziltrietilamonij klorid (0,01 g) je zatim dodan i reakcijska smjesa je zagrijavana na 50 Ā°C tokom 3 dana. Bromoform (0,49 ml), otopina natrij hidroksida (0,226 g) u vodi (1 ml) i etanol (0,1 ml) su dodani i zagrijavanje je nastavljeno tokom 5 dana. Reakcijska smjesa je ostavljena da se ohladi, podijeljena je izmeÄu etera i vode i vodena faza je izdvojena i ekstrahirana sa eterom (Ć 2). Kombinirani organski ekstrakti su isprani sa slanom vodom, osuÅ”eni (Na2SO4) i ispareni pod sniženim tlakom, zatim je ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:eter:diklorometan (1:1:2) kao eluanta, praÄeno obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (60:30:10) kao eluanta, radi dobivanja spoja iz naslova kao zelenkasto-žutu gumu. Bromoform (0.49 ml) was added to a mixed solution of the compound from the title preparation 36 (0.530 g) in dichloromethane (3 ml) followed by a solution of sodium hydroxide (0.226 g) in water (1 ml) and ethanol (0.1 ml). Benzyltriethylammonium chloride (0.01 g) was then added and the reaction mixture was heated at 50 Ā°C for 3 days. Bromoform (0.49 ml), a solution of sodium hydroxide (0.226 g) in water (1 ml) and ethanol (0.1 ml) were added and heating was continued for 5 days. The reaction mixture was allowed to cool, partitioned between ether and water and the aqueous phase separated and extracted with ether (Ć2). The combined organic extracts were washed with brine, dried (Na2SO4) and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel, using hexane:ether:dichloromethane (1:1:2) as eluent, followed by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (60:30:10) as eluent, to give the title compound as a greenish-yellow gum.
Ī“ (CDCl3): 1,87 (t, 1H); 2,28 (dd, 1H); 2,84 (dd, 1H); 7,40 (s, 1H); 7,82 (s, 2H). Ī“ (CDCl 3 ): 1.87 (t, 1H); 2.28 (dd, 1H); 2.84 (dd, 1H); 7.40 (s, 1H); 7.82 (s, 2H).
MS (termosprej): M/Z [M+H] 544,6. C14H6Br2Cl2F6N2 +H zahtijeva 544,83. MS (thermospray): M/Z [M+H] 544.6. C14H6Br2Cl2F6N2 +H requires 544.83.
Primjer 30 Example 30
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-fenilpirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-phenylpyrazole
U izmijeÅ”anu otopinu spoja iz naslova pripreme 40 (0,3 g) u diklorometanu (4 ml) dodan je bromoform (1 ml), praÄeno otopinom natrij hidroksida (0,125 g) u vodi (0,1 ml) i etanola (0,1 ml). Benziltrietilamonij klorid (0,022 g) je zatim dodan i reakcijska smjesa je zagrijavana na 50 Ā°C tokom 5 dana, ostavljena je da se ohladi i podijeljena izmeÄu diklorometana (10 ml) i vode (10 ml). Organska faza je izdvojena, isprana sa vodom, osuÅ”ena (MgSO4) i isparena pod sniženim tlakom, zatim je ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu (70 g), koristeÄi gradijent elucije heksan:etera (100:0 do 95:5 do 90:10 do 0:100), praÄeno obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (60:30:10) kao eluanta. Zahtijevane frakcije iz HPLC stupca bile su koncentrirane i ekstrahirane sa diklorometanom (3 Ć 20 ml). SuÅ”enje zaleÄivanjem kombiniranih ekstrakata dalo je spoj iz naslova kao sasvim bijeli Ävrsti proizvod, t.t. 47-48 Ā°C. Bromoform (1 ml) was added to a mixed solution of the compound from the title preparation 40 (0.3 g) in dichloromethane (4 ml), followed by a solution of sodium hydroxide (0.125 g) in water (0.1 ml) and ethanol (0.1 ml). Benzyltriethylammonium chloride (0.022 g) was then added and the reaction mixture was heated at 50 Ā°C for 5 days, allowed to cool and partitioned between dichloromethane (10 ml) and water (10 ml). The organic phase was separated, washed with water, dried (MgSO4) and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel (70 g), using a gradient elution of hexane:ether (100:0 to 95:5 to 90:10 to 0:100), followed by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (60:30:10) as eluent. The required fractions from the HPLC column were concentrated and extracted with dichloromethane (3 Ć 20 ml). Freeze drying of the combined extracts gave the title compound as an off-white solid, m.p. 47-48 Ā°C.
Ī“ (CDCl3): 1,86 (t, 1H); 2,22 (dd, 1H); 2,80 (dd, 1H); 7,35 (s, 1H); 7,40-7,60 (m, 3H); 7,75 (s, 2H); 7,92 (d, 2H). Ī“ (CDCl 3 ): 1.86 (t, 1H); 2.22 (dd, 1H); 2.80 (dd, 1H); 7.35 (s, 1H); 7.40-7.60 (m, 3H); 7.75 (s, 2H); 7.92 (d, 2H).
MS (termosprej): M/Z [M+H] 553,5. MS (thermospray): M/Z [M+H] 553.5.
C19H11Br2Cl2F3N2 +H zahtijeva 552,87. C19H11Br2Cl2F3N2 +H requires 552.87.
Primjer 31 Example 31
4-(1-klorodifluorometilciklopropil)-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 4-(1-chlorodifluoromethylcyclopropyl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Dobiven iz spoja iz naslova pripreme 44 analogno sa primjerom 27, ali zagrijavajuÄi tokom 4 sata, koristeÄi heksan:eter (8:1) kao kromatografskog eluanta i bez slijedeÄe kristalizacije, kao bijeli Ävrsti proizvod, t.t. 124-125 Ā°C. Obtained from the title compound of Preparation 44 analogously to Example 27, but heating for 4 hours, using hexane:ether (8:1) as chromatographic eluent and without further crystallization, as a white solid product, m.p. 124-125 Ā°C.
Ī“ (CDCl3): 1,24 (m, 2H); 1,58 (m, 2H); 7,74 (s, 1H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 1.24 (m, 2H); 1.58 (m, 2H); 7.74 (s, 1H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+NH4] 446,9. MS (thermospray): M/Z [M+NH 4 ] 446.9.
C15H7Cl3F5N3 +NH4 zahtijeva 447,0. C15H7Cl3F5N3 +NH4 requires 447.0.
Primjer 32 Example 32
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(1-etilciklopropil)-pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-ethylcyclopropyl)-pyrazole
0,467 M otopine diazometana u eteru (30 ml) dodana je tokom 2 minuta u izmijeÅ”anu otopinu spoja iz naslova pripreme 47 (3 g) i paladij(II) acetata (0,025 g) u eteru (5 ml) i rezultirajuÄa smjesa je mijeÅ”ana na sobnoj temperaturi tokom 18 sati. Reakcijska smjesa je filtrirana, tretirana sa dodatnim koliÄinama eterske otopine diazometana (30 ml) i paladij(II) acetata (0,025 g), izmijeÅ”ana je tokom 4 sata joÅ”, filtrirana zatim je dalje tretirana sa eterskom otopinom diazometana (30 ml) i paladij(II) acetatom (0,025 g), mijeÅ”ana je joÅ” 40 minuta, filtrirana zatim je dalje tretirana sa eterskom otopinom diazometana (30 ml) i paladij(II) acetatom (0,025 g), mijeÅ”ana je joÅ” 88 sati, filtrirana zatim je dalje tretirana sa eterskom otopinom diazometana (30 ml) i paladij(II) acetatom (0,025 g), mijeÅ”ana je tokom joÅ” 2 sata, filtrirana, zatim dalje tretirana sa eterskom otopinom diazometana (30 ml) i paladij(II) acetatom (0,025 g), mijeÅ”ana je tokom joÅ” 18 sati i zatim isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda (60:40) kao eluanta, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 118-119 Ā°C. A 0.467 M solution of diazomethane in ether (30 ml) was added over 2 minutes to a mixed solution of the title compound 47 (3 g) and palladium(II) acetate (0.025 g) in ether (5 ml) and the resulting mixture was stirred at room temperature. temperature for 18 hours. The reaction mixture was filtered, treated with additional amounts of ethereal solution of diazomethane (30 ml) and palladium(II) acetate (0.025 g), stirred for another 4 hours, filtered, then further treated with ethereal solution of diazomethane (30 ml) and palladium ( II) with acetate (0.025 g), stirred for another 40 minutes, filtered, then further treated with an ethereal solution of diazomethane (30 ml) and palladium(II) acetate (0.025 g), stirred for another 88 hours, filtered, then further treated with with an ethereal solution of diazomethane (30 ml) and palladium(II) acetate (0.025 g), stirred for another 2 hours, filtered, then further treated with an ethereal solution of diazomethane (30 ml) and palladium(II) acetate (0.025 g), stirred for another 18 hours and then evaporated under reduced pressure. The residue was purified by reverse phase HPLC on C18 silica, using acetonitrile:water (60:40) as eluent, to afford the title compound as a white solid, m.p. 118-119 Ā°C.
Ī“ (CDCl3): 0,80 (m, 2H); 0,90 (m, 5H); 1,63 (m, 2H); 7,44 (s, 1H); 7,77 (s, 2H). Ī“ (CDCl 3 ): 0.80 (m, 2H); 0.90 (m, 5H); 1.63 (m, 2H); 7.44 (s, 1H); 7.77 (s, 2H).
MS (termosprej): M/Z [M+NH4] 390,8. MS (thermospray): M/Z [M+NH4] 390.8.
C16H12Cl2F3N3 +NH4 zahtijeva 391,1. C16H12Cl2F3N3 +NH4 requires 391.1.
Primjer 33 Example 33
3-ciano-4-(2,2-dibromo-1-etilciklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-cyano-4-(2,2-dibromo-1-ethylcyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Otopina iz spoja iz naslova pripreme 47 (105 mg) i feniltribromometil živa (160 mg) u toluenu (4 ml) zagrijavana je na 70 Ā°C tokom 2 sata, zatim je dodana otopina feniltribromometilžive (180 mg) u toluenu (2 ml) i smjesa je zagrijavana na 70 Ā°C tokom 16 sati, joÅ” feniltribromometilžive (230 mg) je dodano i smjesa je zagrijavana na 70 Ā°C tokom 4 sata, joÅ” feniltribromometilžive (310 mg) je dodano i smjesa je zagrijavana na 70 Ā°C tokom 2 sata, joÅ” feniltribromometilžive (310 mg) je dodano i smjesa je zagrijavana na 70 Ā°C tokom 16 sati, zatim je ostavljena da se ohladi. RezultirajuÄa smjesa je filtrirana preko silikagela (10 g), koristeÄi heksan i zatim dihlorometan kao eluanta, i zatim su zahtijevane frakcije eluata isparene pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (10 g), koristeÄi diklorometa:heksan (1:4) kao eluanta, praÄeno obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (60:30:10) kao eluanta, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 107-108Ā°C. A solution of the compound from the title preparation 47 (105 mg) and phenyltribromomethylmercury (160 mg) in toluene (4 ml) was heated at 70 Ā°C for 2 hours, then a solution of phenyltribromomethylmercury (180 mg) in toluene (2 ml) was added and the mixture was heated at 70 Ā°C for 16 hours, more phenyltribromomethylmercury (230 mg) was added and the mixture was heated at 70 Ā°C for 4 hours, more phenyltribromomethylmercury (310 mg) was added and the mixture was heated at 70 Ā°C for 2 hours , more phenyltribromomethylmercury (310 mg) was added and the mixture was heated at 70 Ā°C for 16 hours, then allowed to cool. The resulting mixture was filtered through silica gel (10 g), using hexane and then dichloromethane as eluent, and then the required eluate fractions were evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (10 g), using dichloromethane:hexane (1:4) as eluant, followed by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (60:30:10) as eluant, for obtaining the title compound as a white solid, m.p. 107-108Ā°C.
Ī“ (CDCl3): 1,04 (t, 3H); 1,90 (m, 2H); 2,19 (m, 2H); 7,62 (s, 2H); 7,79 (s, 2H). Ī“ (CDCl 3 ): 1.04 (t, 3H); 1.90 (m, 2H); 2.19 (m, 2H); 7.62 (s, 2H); 7.79 (s, 2H).
MS (termosprej): M/Z [M+H] 530,0. C16H10Br2Cl2F3N3 +H zahtijeva 529,9. MS (thermospray): M/Z [M+H] 530.0. C16H10Br2Cl2F3N3 +H requires 529.9.
Primjer 34 Example 34
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(1-pentafluoroetilciklopropil)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-pentafluoroethylcyclopropyl)pyrazole
Dobiven je iz spoja iz naslova pripreme 50, analogno sa primjerom 31 ali koristeÄi obrnutu fazu HPLC na C18 silicij dioksidu sa acetonitril:voda:metanolom (60:30:10) kao eluantom, kao bijeli Ävrsti proizvod, t.t. 105-106 Ā°C. It was obtained from the title compound of preparation 50, analogously to example 31 but using reverse phase HPLC on C18 silica with acetonitrile:water:methanol (60:30:10) as eluent, as a white solid product, m.p. 105-106 Ā°C.
Ī“ (CDCl3): 1,24 (m, 2H); 1,55 (m, 2H); 7,67 (s, 1H); 7,77 (s, 2H). Ī“ (CDCl 3 ): 1.24 (m, 2H); 1.55 (m, 2H); 7.67 (s, 1H); 7.77 (s, 2H).
MS (elektrosprej): M/Z [M+H] 464,0. C16H7Cl2F8N3 +H zahtijeva 464,0. MS (electrospray): M/Z [M+H] 464.0. C16H7Cl2F8N3 +H requires 464.0.
Primjer 35 Example 35
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(1-heptafluoropropilciklopropil)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-heptafluoropropylcyclopropyl)pyrazole
Dobiven iz spoja pripreme 53, analogno sa primjerom 31 ali zagrijavajuÄi tokom 3 sata i vrÅ”eÄi poslije-kromatografsku kristalizaciju iz cikloheksana, kao bijeli Ävrsti proizvod, t.t. 95-96 Ā°C. Obtained from the compound of preparation 53, analogously to Example 31 but heating for 3 hours and performing post-chromatographic crystallization from cyclohexane, as a white solid, m.p. 95-96 Ā°C.
Ī“ (CDCl3): 1,23 (m, 2H); 1,54 (m, 2H); 7,65 (s, 1H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 1.23 (m, 2H); 1.54 (m, 2H); 7.65 (s, 1H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+H] 514,2. C17H7Cl2F10N3 +H zahteva 514,0. MS (thermospray): M/Z [M+H] 514.2. C17H7Cl2F10N3 +H requires 514.0.
Primjer 36 Example 36
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(1-trifluorometilciklopropil)pirazol 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-trifluoromethylcyclopropyl)pyrazole
Otopina spoja iz naslova pripreme 55 (130 mg) u smjesi ksilena (8 ml) i toluena (1 ml) zagrijavana je pod blagim refluksom tokom 7 sati, zatim je ostavljena da stoji na sobnoj temperaturi tokom 16 sati. Otapalo je uklonjeno isparavanjem pod sniženim tlakom i rezultirajuÄi talog je proÄiÅ”Äen obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (45:45:10) kao eluanta, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 178-179 Ā°C. A solution of the compound from the title preparation 55 (130 mg) in a mixture of xylene (8 ml) and toluene (1 ml) was heated under gentle reflux for 7 hours, then it was left to stand at room temperature for 16 hours. The solvent was removed by evaporation under reduced pressure and the resulting residue was purified by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (45:45:10) as eluent, to afford the title compound as a white solid, m.p. 178-179 Ā°C.
Ī“ (CDCl3): 1,13 (m, 2H); 1,48 (m, 2H); 3,91 (br.s, 2H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 1.13 (m, 2H); 1.48 (m, 2H); 3.91 (no.s, 2H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+H] 429,1. C15H8Cl2F6N4 +H zahtijeva 429,0. MS (thermospray): M/Z [M+H] 429.1. C15H8Cl2F6N4 +H requires 429.0.
Primjer 37 Example 37
1-[(3-kloro-5-trifluorometil)piridin-2-il]-3-ciano-4-(2,2-dibromociklopropil)pirazol 1-[(3-chloro-5-trifluoromethyl)pyridin-2-yl]-3-cyano-4-(2,2-dibromocyclopropyl)pyrazole
Otopina spoja iz naslova pripreme 58 (0,50 g) i feniltribromometil žive (1,0 g) u toluenu (5 ml) zagrijavana je na 70 Ā°C pod duÅ”ikom tokom 1,5 sata. JoÅ” feniltribromometilžive (0,50 g) je dodano i zagrijavanje je nastavljeno tokom slijedeÄa 72 sata. RezultirajuÄa smjesa je ostavljena da se ohladi, podijeljena je izmeÄu etera i vode, i vodena faza je izdvojena i ekstrahirana sa eterom (Ć 2). Kombinirani ekstrakti su isprani uzastopno sa vodom i slanom vodom, osuÅ”eni (MgSO4) i ispareni pod sniženim tlakom. Sirovi proizvod (0,50 g), smeÄe ulje, je proÄiÅ”Äeno kromatografijom stupca na silikagelu, koristeÄi heksan:etil acetat (9:1) kao eluanta, radi dobivanja spoja iz naslova kao žuti Ävrsti proizvod, t.t. 81-83 Ā°C. A solution of the title compound 58 (0.50 g) and phenyltribromomethylmercury (1.0 g) in toluene (5 ml) was heated to 70 Ā°C under nitrogen for 1.5 hours. More phenyltribromomethylmercury (0.50 g) was added and heating was continued for the next 72 hours. The resulting mixture was allowed to cool, partitioned between ether and water, and the aqueous phase separated and extracted with ether (Ć2). The combined extracts were washed sequentially with water and brine, dried (MgSO4) and evaporated under reduced pressure. The crude product (0.50 g), a brown oil, was purified by column chromatography on silica gel using hexane:ethyl acetate (9:1) as eluent to give the title compound as a yellow solid, m.p. 81-83 Ā°C.
Ī“ (CDCl3): 2,05 (t, 1H); 2,33 (dd, 1H); 2,85 (dd, 1H); 8,20 (s, 1H); 8,23 (s, 1H); 8,70 (s, 1H). Ī“ (CDCl 3 ): 2.05 (t, 1H); 2.33 (dd, 1H); 2.85 (dd, 1H); 8.20 (s, 1H); 8.23 (s, 1H); 8.70 (s, 1H).
MS (termosprej): M/Z [M+H] 467,9. MS (thermospray): M/Z [M+H] 467.9.
C13H6Br2ClF3N4 +H zahtijeva 467,9. C13H6Br2ClF3N4 +H requires 467.9.
Primjer 38 Example 38
3-acetil-4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 3-acetyl-4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Otopina spoja iz naslova primjera 2 (3,42 g) u eteru (25 ml) dodana je u izmijeÅ”anu, ledeno-ohlaÄenu smjesu 3,0 M otopine metilmagnezij jodida u eteru (2,26 ml) i nevodenog etera (25 ml) pod duÅ”ikom, dok se održava reakcijska temperatura ispod 2 Ā°C. Reakcijska smjesa je ostavljena da se zagrije na sobnu temperaturu, zagrijavana je pod refluksom tokom 2 sata i zatim je tretirana sa joÅ” (0,5 ml) 3M eterske otopine metilmagnezij jodida. Ova smjesa je zagrijavana pod refluksom tokom 1 sata i zatim je mijeÅ”ana na sobnoj temperaturi tokom 18 sati. Daljnja koliÄina (1 ml) eterske otopine metilmagnezij jodida je dodana i rezultirajuÄa smjesa je zagrijavana pod refluksom tokom 3 sata, zatim je sipana u izmijeÅ”anu smjesu koncentrirane klorovodiÄne kiseline (2 ml) i leda (10 g). Ekstrakcija sa eterom (Ć 3), praÄeno ispiranjem kombiniranih ekstrakata sa slanom vodom, suÅ”enjem (MgSO4) i isparavanjem pod sniženim tlakom, dala je sirovi proizvod koji je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:diklorometan (1:1) kao eluanta, praÄeno kristalizacijom iz heksana, radi dobivanja spoja iz naslova kao blijedo žutog proizvoda, t.t. 149,5-150,3 Ā°C. A solution of the title compound of Example 2 (3.42 g) in ether (25 ml) was added to a stirred, ice-cooled mixture of a 3.0 M solution of methylmagnesium iodide in ether (2.26 ml) and anhydrous ether (25 ml) under with nitrogen, while maintaining the reaction temperature below 2 Ā°C. The reaction mixture was allowed to warm to room temperature, heated under reflux for 2 hours and then treated with more (0.5 ml) of 3M ethereal methylmagnesium iodide. This mixture was heated under reflux for 1 hour and then stirred at room temperature for 18 hours. A further amount (1 ml) of ethereal solution of methylmagnesium iodide was added and the resulting mixture was heated under reflux for 3 hours, then poured into a stirred mixture of concentrated hydrochloric acid (2 ml) and ice (10 g). Extraction with ether (Ć 3), followed by washing the combined extracts with brine, drying (MgSO4) and evaporation under reduced pressure gave the crude product which was purified by column chromatography on silica gel, using hexane:dichloromethane (1:1) as eluent, followed by crystallization from hexane to give the title compound as a pale yellow product, m.p. 149.5-150.3 Ā°C.
Ī“ (CDCl3): 1,78 (dd, 1H); 2,24 (dd, 1H); 2,69 (s, 3H); 3,37 (dd, 1H); 7,34 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 1.78 (dd, 1H); 2.24 (dd, 1H); 2.69 (s, 3H); 3.37 (dd, 1H); 7.34 (s, 1H); 7.78 (s, 2H).
MS (termosprej): M/Z [M+NH4] 536,3. MS (thermospray): M/Z [M+NH 4 ] 536.3.
C15H9Br2Cl2F3N2O+NH4 zahtijeva 535,88. C15H9Br2Cl2F3N2O+NH4 requires 535.88.
Primjer 39 Example 39
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-(1-hidroksietil)pirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(1-hydroxyethyl)pyrazole
1M otopina boran:tetrahidrofuran kompleksa u tetrahidrofuranu (4,61 ml) dodana je u izmijeÅ”anu otopinu spoja iz naslova primjera 38 (0,40 g) u nevodenom tetrahidrofuranu (5 ml) na oko -50 Ā°C pod duÅ”ikom. Reakcijska smjesa je ostavljena da se zagrije na sobnu temperaturu, mijeÅ”ana je slijedeÄih 4 sata i zatim isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:eter (3:1) kao eluant, radi dobivanja spoja iz naslova kao uljasti bijeli Ävrsti proizvod. A 1M solution of the borane:tetrahydrofuran complex in tetrahydrofuran (4.61 ml) was added to a stirred solution of the title compound of Example 38 (0.40 g) in anhydrous tetrahydrofuran (5 ml) at about -50 Ā°C under nitrogen. The reaction mixture was allowed to warm to room temperature, stirred for a further 4 hours and then evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using hexane:ether (3:1) as eluent to give the title compound as an oily white solid.
Ī“ (CDCl3): 1,55 (s, 1H); 1,75 (d, 3H); 1,80 (t, 1H); 2,20 (dd, 1H); 2,95 (dd, 1H); 5,20 (m, 1H); 7,25 (s, 1H); 7,70 (s, 2H). Ī“ (CDCl 3 ): 1.55 (s, 1H); 1.75 (d, 3H); 1.80 (t, 1H); 2.20 (dd, 1H); 2.95 (dd, 1H); 5.20 (m, 1H); 7.25 (s, 1H); 7.70 (s, 2H).
MS (termosprej): M/Z [M+H] 521,0. MS (thermospray): M/Z [M+H] 521.0.
C15H11Br2Cl2F3N2O+H zahtijeva 520,86. C15H11Br2Cl2F3N2O+H requires 520.86.
Primjer 40 Example 40
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-etilpirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-ethylpyrazole
Trietilsilan (0,22 ml) je dodan u izmijeÅ”anu otopinu spoja iz naslova primjera 39 (0,18 g) u diklorometanu (5 ml), na oko -75 Ā°C, dok se reakcijska temperatura održava ispod -70 Ā°C. Bor trifluorid dietil eterat (0,17 ml) je dodan i reakcijska smjesa je ostavljena da se zagrije na sobnu temperaturu, zatim je mijeÅ”ana tokom slijedeÄa 24 sata. Dalje, smjesa je ohlaÄena na oko -70 Ā°C, dodano je joÅ” trietilsilana (0,22 ml) i bor trifluorid dietil eterata (0,17 ml), kada za hlaÄenje je uklonjena i mijeÅ”anje je nastavljeno na sobnoj temperaturi tokom 4 dana. RezultirajuÄa smjesa je isprana sa razblaženom klorovodikovom kiselinom i vodena faza je ekstrahirana sa diklorometanom (Ć 2). Kombinirane organske otopine su isprane sa slanom vodom, osuÅ”ene (Na2SO4) i isparene pod sniženim pritiskom, zatim je talog proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:eter (2:1) kao eluanta, radi dobivanja spoja iz naslova kao bezbojno ulje. Triethylsilane (0.22 ml) was added to a stirred solution of the title compound of Example 39 (0.18 g) in dichloromethane (5 ml) at about -75 Ā°C while maintaining the reaction temperature below -70 Ā°C. Boron trifluoride diethyl etherate (0.17 mL) was added and the reaction mixture was allowed to warm to room temperature, then stirred for the next 24 hours. Next, the mixture was cooled to about -70 Ā°C, more triethylsilane (0.22 ml) and boron trifluoride diethyl etherate (0.17 ml) were added, the cooling tub was removed and stirring was continued at room temperature for 4 days. The resulting mixture was washed with dilute hydrochloric acid and the aqueous phase was extracted with dichloromethane (Ć2). The combined organic solutions were washed with brine, dried (Na2SO4) and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel, using hexane:ether (2:1) as eluent, to give the title compound as a colorless oil.
Ī“ (CDCl3): 1,45 (t, 3H); 1,80 (t, 1H); 2,20 (dd, 1H); 2,65 (dd, 1H); 2,85 (q, 2H); 7,20 (s, 1H); 7,70 (s, 2H). Ī“ (CDCl 3 ): 1.45 (t, 3H); 1.80 (t, 1H); 2.20 (dd, 1H); 2.65 (dd, 1H); 2.85 (q, 2H); 7.20 (s, 1H); 7.70 (s, 2H).
MS (termosprej): M/Z [M+H] 504,9. MS (thermospray): M/Z [M+H] 504.9.
C15H11Br2Cl2F3N2 +H zahtijeva 504,87. C15H11Br2Cl2F3N2 +H requires 504.87.
Primjer 41 Example 41
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-(2-hidroksiprop-2-il)pirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(2-hydroxyprop-2-yl)pyrazole
Otopina spoja iz naslova primjera 38 (0,30 g) u eteru (5 ml) dodana je u izmijeÅ”anu, ledeno-hladnu smjesu 3,0 M otopine metilmagnezij jodida (0,21 ml) i nevodenog etera (5 ml) pod duÅ”ikom, dok se reakcijska temperatura održava ispod 2 Ā°C. Reakcijska smjesa je ostavljena da se zagrije na sobnu temperaturu, zagrijavana je pod refluksom tokom 1 sata, ostavljena je da se ohladi, zatim je sipana u izmijeÅ”anu smjesu koncentrirane klorovodiÄne kiseline (2 ml) i leda (10 g). Ekstrakcija sa eterom (Ć 3), praÄena ispiranjem kombiniranih ekstrakata sa slanom vodom, suÅ”enjem (MgSO4) i isparavanjem pod sniženim tlakom, dala je sirovi proizvod koji je kristaliziran iz toluena radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 132,1-132,7 Ā°C. A solution of the title compound of Example 38 (0.30 g) in ether (5 ml) was added to a stirred, ice-cold mixture of a 3.0 M solution of methylmagnesium iodide (0.21 ml) and anhydrous ether (5 ml) under nitrogen, while the reaction temperature is kept below 2 Ā°C. The reaction mixture was allowed to warm to room temperature, heated under reflux for 1 hour, allowed to cool, then poured into a stirred mixture of concentrated hydrochloric acid (2 ml) and ice (10 g). Extraction with ether (Ć 3), followed by washing the combined extracts with brine, drying (MgSO 4 ) and evaporation under reduced pressure gave the crude product which was crystallized from toluene to give the title compound as a white solid, m.p. 132.1-132.7 Ā°C.
Ī“ (CDCl3): 1,80 (s, 6H); 1,82 (t, 1H); 2,20 (dd, 1H); 2,55 (s, 1H); 3,05 (dd, 1H); 7,20 (s, 1H); 7,70 (s, 2H). Ī“ (CDCl 3 ): 1.80 (s, 6H); 1.82 (t, 1H); 2.20 (dd, 1H); 2.55 (s, 1H); 3.05 (dd, 1H); 7.20 (s, 1H); 7.70 (s, 2H).
MS (termosprej): M/Z [M+H] 534,4. MS (thermospray): M/Z [M+H] 534.4.
C16H13Br2Cl2F3N2O+H zahteva 534,88. C16H13Br2Cl2F3N2O+H requires 534.88.
Primjer 42 Example 42
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-prop-2-il)pirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-prop-2-yl)pyrazole
Trietilsilan (0,14 ml) je dodan u izmijeÅ”anu otopinu spoja iz naslova primjera 41 (0,115 g) u diklorometanu (5 ml) na oko -75 Ā°C, dok je reakcijska temperatura održavana ispod -70 Ā°C. Bor trifluorid dietil eterat (0,11 ml) je dodan i reakcijska smjesa je držana na oko -70 Ā°C tokom 2,5 sata, prije nego Å”to je ostavljena da se zagrije na sobnu temperaturu. Nakon daljnja 24 sata, smjesa je oprana sa razblaženom klorovodikovom kiselinom i vodena faza je zatim ekstrahirana sa eterom (Ć 2). Kombinirane organske otopine su isprane sa slanom vodom, osuÅ”ene (Na2SO4) i isparene pod sniženim tlakom radi dobivanja sirovog proizvoda koji je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:eter (4:1) kao eluant, radi dobivanja spoja iz naslova kao bezbojno ulje. Triethylsilane (0.14 ml) was added to a stirred solution of the title compound of Example 41 (0.115 g) in dichloromethane (5 ml) at about -75 Ā°C while the reaction temperature was maintained below -70 Ā°C. Boron trifluoride diethyl etherate (0.11 ml) was added and the reaction mixture was kept at about -70 Ā°C for 2.5 hours, before being allowed to warm to room temperature. After a further 24 hours, the mixture was washed with dilute hydrochloric acid and the aqueous phase was then extracted with ether (Ć2). The combined organic solutions were washed with brine, dried (Na2SO4) and evaporated under reduced pressure to give the crude product which was purified by column chromatography on silica gel, using hexane:ether (4:1) as eluent, to give the title compound as a colorless oil. .
Ī“ (CDCl3): 1,40 (d, 6H); 1,80 (t, 1H); 2,20 (dd, 1H); 2,70 (dd, 1H); 3,20 (sept., 1H); 7,15 (s, 1H); 7,70 (s, 2H). Ī“ (CDCl 3 ): 1.40 (d, 6H); 1.80 (t, 1H); 2.20 (dd, 1H); 2.70 (dd, 1H); 3.20 (Sept., 1H); 7.15 (s, 1H); 7.70 (s, 2H).
MS (termosprej): M/Z [M+H] 518,4. MS (thermospray): M/Z [M+H] 518.4.
C16H13Br2Cl2F3N2 +H zahtijeva 518,89. C16H13Br2Cl2F3N2 +H requires 518.89.
Primjer 43 Example 43
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-formilpirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-formylpyrazole
1M otopina diizobutilaluminij hidrid u heksanu (1,5 ml) dodana je ukapavanjem tokom 5 minuta u izmijeÅ”anu, ledeno-ohlaÄenu otopinu spoja iz naslova primjera 2 (0,50 g) u nevodenom tetrahidrofuranu (15 ml). Nakon 1 sata, reakcijska smjesa je tretirana sa jednom daljnjom koliÄinom (2,25 ml) otopine hidrida, mijeÅ”ana je tokom 18 sati i zatim je sipana u zakiseljen vodeni metanol. Ova smjesa je ekstrahirana sa eterom (Ć 2), zatim su kombinirani organski ekstrakti isprani sukcesivno sa vodom i slanom vodom, osuÅ”eni (MgSO4) i ispareni pod sniženim tlakom. RezultirajuÄi talog je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:etil acetat (9:1) kao eluant, radi dobivanja spoja iz naslova kao ulje. A 1M solution of diisobutylaluminum hydride in hexane (1.5 ml) was added dropwise over 5 minutes to a stirred, ice-cooled solution of the title compound of Example 2 (0.50 g) in anhydrous tetrahydrofuran (15 ml). After 1 hour, the reaction mixture was treated with an additional amount (2.25 mL) of the hydride solution, stirred for 18 hours, and then poured into acidified aqueous methanol. This mixture was extracted with ether (Ć2), then the combined organic extracts were washed successively with water and brine, dried (MgSO4) and evaporated under reduced pressure. The resulting precipitate was purified by silica gel column chromatography using hexane:ethyl acetate (9:1) as eluent to afford the title compound as an oil.
Ī“ (CDCl3): 1,80 (dd, 1H); 2,28 (dd, 1H); 3,32 (dd, 1H); 7,39 (s, 1H); 7,78 (s, 2H); 10,19 (s, 1H). Ī“ (CDCl 3 ): 1.80 (dd, 1H); 2.28 (dd, 1H); 3.32 (dd, 1H); 7.39 (s, 1H); 7.78 (s, 2H); 10.19 (s, 1H).
MS (termosprej): M/Z [M+H] 504,7. MS (thermospray): M/Z [M+H] 504.7.
C14H7Br2Cl2F3N2O+H zahtijeva 504,83. C14H7Br2Cl2F3N2O+H requires 504.83.
Primjer 44 Example 44
4-(2,2-dibromociklopropil)-1-(2,6-dikloro-4-trifluorometilfenil)-3-difluorometilpirazol 4-(2,2-dibromocyclopropyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-difluoromethylpyrazole
Dietilaminosumpor trifluorid (0,13 g) dodan je u izmijeÅ”anu otopinu spoja iz naslova primjera 43 (0,20 g) u diklorometanu (5 ml). Nakon daljnja 3 sata na sobnoj temperaturi, reakcijska smjesa je razblažena sa diklorometanom, isprana sa vodom (Ć 2), osuÅ”ena (MgSO4) i isparena pod sniženim tlakom. Talog je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:etil acetat (19:1) kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 99-101 Ā°C. Diethylaminosulfur trifluoride (0.13 g) was added to a stirred solution of the title compound of Example 43 (0.20 g) in dichloromethane (5 ml). After a further 3 hours at room temperature, the reaction mixture was diluted with dichloromethane, washed with water (Ć2), dried (MgSO 4 ) and evaporated under reduced pressure. The residue was purified by silica gel column chromatography using hexane:ethyl acetate (19:1) as eluent to give the title compound as a white solid, m.p. 99-101 Ā°C.
Ī“ (CDCl3): 1,85 (t, 1H); 2,25 (dd, 1H); 2,95 (dd, 1H); 6,87 (t, 1H); 7,38 (s, 1H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 1.85 (t, 1H); 2.25 (dd, 1H); 2.95 (dd, 1H); 6.87 (t, 1H); 7.38 (s, 1H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+H] 526,5. MS (thermospray): M/Z [M+H] 526.5.
C14H7Br2Cl2F5N2 +H zahtijeva 526,84. C14H7Br2Cl2F5N2 +H requires 526.84.
Primjer 45 Example 45
4-(2,2-dibromociklopropil)-3-diklorometil1-(2,6-dikloro-4-trifluorometilfenil)pirazol 4-(2,2-dibromocyclopropyl)-3-dichloromethyl1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Fosfor pentaklorid (0,17 g) je dodan u izmijeÅ”anu otopinu spoja iz naslova primjera 43 (0,20 g) u eteru (10 ml). Nakon daljnja 24 sata dodano je joÅ” fosfor pentaklorida (0,17 g) i reakcijska smjesa je mijeÅ”ana daljnja 24 sata, prije isparavanja pod sniženim tlakom. ProÄiÅ”Äavanje taloga kromatografijom stupca na silikagelu, koristeÄi heksan:etil acetat (19:1) kao eluant, dalo je spoj iz naslova kao bijeli Ävrsti proizvod, t.t. 87-89 Ā°C. Phosphorus pentachloride (0.17 g) was added to a stirred solution of the title compound of Example 43 (0.20 g) in ether (10 ml). After a further 24 hours more phosphorus pentachloride (0.17 g) was added and the reaction mixture was stirred for a further 24 hours, before evaporation under reduced pressure. Purification of the residue by column chromatography on silica gel using hexane:ethyl acetate (19:1) as eluent gave the title compound as a white solid, m.p. 87-89 Ā°C.
Ī“ (CDCl3): 1,90 (t, 1H); 2,29 (dd, 1H); 3,12 (dd, 1H); 6,96 (s, 1H); 7,30 (s, 1H); 7,72 (s, 2H). Ī“ (CDCl 3 ): 1.90 (t, 1H); 2.29 (dd, 1H); 3.12 (dd, 1H); 6.96 (s, 1H); 7.30 (s, 1H); 7.72 (s, 2H).
MS (APCI): M/Z [M+H] 559,2. MS (APCI): M/Z [M+H] 559.2.
C14H7Br2Cl4F3N2 +H zahtijeva 558,78. C14H7Br2Cl4F3N2 +H requires 558.78.
Primjer 46 Example 46
3-ciano-4-(2,2-dibromociklopropil)-1-(2,4,6-triklorofenil)pirazol 3-cyano-4-(2,2-dibromocyclopropyl)-1-(2,4,6-trichlorophenyl)pyrazole
Smjesa spoja iz naslova pripreme 61 (2,0 g), 96 %-nog bromoforma stabiliziranog sa 1 do 3 % etanola (6,5 ml), natrij hidroksida (1,0 g), vode (1,0 ml), etanola (0,14 ml), diklorometana (6,5 ml) i benziltrietilamonij klorida (80 mg) brzo je mijeÅ”ana pod blagim refluksom na oko 40 Ā°C tokom 6 sati, zatim na sobnoj temperaturi tokom 18 sati i opet na oko 40 Ā°C tokom 6 sati. Dodano je joÅ” natrij hidroksida (0,3 g), vode (0,6 ml) i katalizatora kvaternarne amonij soli (130 mg) i reakcijska smjesa je jako mijeÅ”ana na oko 40 Ā°C tokom 6 sati i zatim na sobnoj temperaturi tokom 18 sati. Dodano je joÅ” katalizatora (100 mg) i reakcijska smjesa je mijeÅ”ana na oko 40Ā°C tokom 6 sati i zatim na sobnoj temperaturi tokom 66 sati. Dodano je joÅ” katalizatora (100 mg) i joÅ” diklorometana (2,0 ml) i reakcijska smjesa je mijeÅ”ana na oko 40 Ā°C tokom 6 sati, na sobnoj temperaturi tokom 18 sati, na oko 40 Ā°C tokom 7 sati, na sobnoj temperaturi tokom 18 sati, na oko 40 Ā°C tokom 7 sati i na sobnoj temperaturi tokom 18 sati. KonaÄno, dodano je joÅ” 96 %-nog bromoforma (3,0 ml), 50 % vodene otopine natrij hidroksida (0,5 ml), diklorometana (3,0 ml) i katalizatora (150 mg) i rezultirajuÄa smjesa je mijeÅ”ana na sobnoj temperaturi tokom jednog tjedna, zatim je podijeljena izmeÄu diklorometana (100 ml) i vode (50 ml). Izdvojena organska faza je isprana sa vodom (50 ml), osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom radi dobivanja crne gume koja je proÄiÅ”Äena kromatografijom stupca na silikagelu (100 g), koristeÄi heksan i zatim heksan:eter:dihlorometan (8:1:1) kao eluant, radi dobivanja spoja iz naslova kao vrlo blijedo žutog Ävrstog proizvoda, t.t. 164 Ā°C. A mixture of the compound from the title preparation 61 (2.0 g), 96% bromoform stabilized with 1 to 3% ethanol (6.5 ml), sodium hydroxide (1.0 g), water (1.0 ml), ethanol (0.14 ml), dichloromethane (6.5 ml) and benzyltriethylammonium chloride (80 mg) was stirred rapidly under gentle reflux at about 40 Ā°C for 6 hours, then at room temperature for 18 hours and again at about 40 Ā°C during 6 hours. More sodium hydroxide (0.3 g), water (0.6 ml) and quaternary ammonium salt catalyst (130 mg) were added and the reaction mixture was vigorously stirred at about 40 Ā°C for 6 hours and then at room temperature for 18 hours. . More catalyst (100 mg) was added and the reaction mixture was stirred at about 40Ā°C for 6 hours and then at room temperature for 66 hours. More catalyst (100 mg) and more dichloromethane (2.0 ml) were added and the reaction mixture was stirred at about 40 Ā°C for 6 hours, at room temperature for 18 hours, at about 40 Ā°C for 7 hours, at room temperature for 18 hours, at around 40 Ā°C for 7 hours and at room temperature for 18 hours. Finally, more 96% bromoform (3.0 mL), 50% aqueous sodium hydroxide solution (0.5 mL), dichloromethane (3.0 mL), and catalyst (150 mg) were added and the resulting mixture was stirred at room temperature. temperature for one week, then partitioned between dichloromethane (100 ml) and water (50 ml). The separated organic phase was washed with water (50 ml), dried (Na2SO4) and evaporated under reduced pressure to give a black gum which was purified by column chromatography on silica gel (100 g) using hexane and then hexane:ether:dichloromethane (8:1 :1) as eluent, to give the title compound as a very pale yellow solid, m.p. 164 Ā°C.
Ī“ (CDCl3): 2,02 (t, 1H); 2,34 (dd, 1H); 2,87 (dd, 1H); 7,48 (s, 1H); 7,51 (s, 2H). Ī“ (CDCl 3 ): 2.02 (t, 1H); 2.34 (dd, 1H); 2.87 (dd, 1H); 7.48 (s, 1H); 7.51 (s, 2H).
MS (termosprej): M/Z [M+NH4] 484,6. MS (thermospray): M/Z [M+NH 4 ] 484.6.
C13H6Br2Cl3N3 +NH4 zahtijeva 484,8. C13H6Br2Cl3N3 +NH4 requires 484.8.
Primjer 47 Example 47
3-ciano-4-(2,2-diklorociklopropil)-1-(2,4,6-triklorofenil)pirazol 3-cyano-4-(2,2-dichlorocyclopropyl)-1-(2,4,6-trichlorophenyl)pyrazole
Smjesa spoja iz naslova pripreme 61 (2,0 g), kloroforma (6,0 ml), natrij hidroksida (1,0 g), vode (1,0 ml), etanola (0,2 ml), diklorometana (6,5 ml) i benziltrietilamonij klorida (150 mg) brzo je mijeÅ”ana na oko 40 Ā°C tokom 66 sati. Dodano je joÅ” natrij hidroksida (0,5 g), vode (1,0 ml), diklorometana (4 ml) i katalizatora kvaternarne amonij soli (180 mg) i reakcijska smjesa je mijeÅ”ana na oko 40 Ā°C tokom 90 sati. Dodano je joÅ” katalizatora (150 mg), diklormetana (5,0 ml), 50 % vodene otopine natrij hidroksida (0,5 ml) i kloroforma (3,0 ml) i rezultirajuÄa smjesa je mijeÅ”ana na oko 36 Ā°C tokom 10 dana, zatim je podijeljena izmeÄu diklorometana (100 ml) i vode (50 ml). Izdvojena organska faza je isprana sa vodom (50 ml), osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom radi dobivanja crne gume koja je proÄiÅ”Äena kromatografijom stupca na silikagelu (80 g), koristeÄi heksan:eter:diklorometan (8:1:1) kao eluant, radi dobivanja spoja iz naslova kao blijedo žutog Ävrstog proizvoda, t.t. 157,8 Ā°C. A mixture of the compound from the title of preparation 61 (2.0 g), chloroform (6.0 ml), sodium hydroxide (1.0 g), water (1.0 ml), ethanol (0.2 ml), dichloromethane (6, 5 ml) and benzyltriethylammonium chloride (150 mg) was rapidly stirred at about 40 Ā°C for 66 hours. More sodium hydroxide (0.5 g), water (1.0 ml), dichloromethane (4 ml) and quaternary ammonium salt catalyst (180 mg) were added and the reaction mixture was stirred at about 40 Ā°C for 90 hours. More catalyst (150 mg), dichloromethane (5.0 ml), 50% aqueous sodium hydroxide solution (0.5 ml) and chloroform (3.0 ml) were added and the resulting mixture was stirred at about 36 Ā°C for 10 days. , then partitioned between dichloromethane (100 ml) and water (50 ml). The separated organic phase was washed with water (50 ml), dried (Na2SO4) and evaporated under reduced pressure to give a black gum which was purified by column chromatography on silica gel (80 g) using hexane:ether:dichloromethane (8:1:1). as eluent, to give the title compound as a pale yellow solid, m.p. 157.8 Ā°C.
Ī“ (CDCl3): 1,85 (t, 1H); 2,19 (dd, 1H); 2,85 (dd, 1H); 7,49 (s, 1H); 7,52 (s, 2H). Ī“ (CDCl 3 ): 1.85 (t, 1H); 2.19 (dd, 1H); 2.85 (dd, 1H); 7.49 (s, 1H); 7.52 (s, 2H).
MS (termosprej): [M/Z+NH4] 396,8. MS (thermospray): [M/Z+NH 4 ] 396.8.
C13H6Cl5N3 +NH4 zahtijeva 396,9. C13H6Cl5N3 +NH4 requires 396.9.
Primjer 48 Example 48
5-amino-3-ciano-4-(2,2-diklorociklopropil)-1-(2,6-dikloro-4-pentafluorotiofenil)pirazol 5-amino-3-cyano-4-(2,2-dichlorocyclopropyl)-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole
Jako izmijeÅ”ana smjesa 5-amino-3-ciano-1-(2,6-dikloro-4-pentafluorotiofenil)-4-etenilpirazola (WO-A-97/ 07102; 0,50 g), kloroforma (3,0 ml), otopine natrij hidroksida (0,25 g) u vodi (0,25 ml), etanola (2 kapi), diklorometana (2,0 ml) i benziltrietilamonij klorida (25 mg) zagrijavana je pod refluksom tokom 18 sati, zatim je dodano joÅ” kloroforma (3,0 ml) i katalizatora kvaternarne amonij soli (25 mg) i mijeÅ”anje pod refluksom je nastavljeno tokom 78 sati. Dodano je joÅ” kloroforma (3,0 ml) i katalizatora (25 mg) i rezultirajuÄa smjesa je mijeÅ”ana pod refluksom tokom 4 dana, zatim je podijeljena izmeÄu diklorometana (30 ml) i vode (30 ml). Izdvojena organska faza je isprana sa vodom (2 Ć 20 ml) i zasiÄenom slanom vodom (20 ml), osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom radi dobivanja tamnog smeÄeg ulja. Ovaj sirovi materijal je proÄiÅ”Äen kako slijedi: A highly stirred mixture of 5-amino-3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)-4-ethenylpyrazole (WO-A-97/07102; 0.50 g), chloroform (3.0 ml) , a solution of sodium hydroxide (0.25 g) in water (0.25 ml), ethanol (2 drops), dichloromethane (2.0 ml) and benzyltriethylammonium chloride (25 mg) was heated under reflux for 18 hours, then added more chloroform (3.0 ml) and quaternary ammonium salt catalyst (25 mg) and stirring under reflux was continued for 78 hours. More chloroform (3.0 ml) and catalyst (25 mg) were added and the resulting mixture was stirred under reflux for 4 days, then partitioned between dichloromethane (30 ml) and water (30 ml). The separated organic phase was washed with water (2 x 20 ml) and saturated brine (20 ml), dried (Na 2 SO 4 ) and evaporated under reduced pressure to give a dark brown oil. This crude material was purified as follows:
(i) pred-apsorpcija na silikagelu (1,5 g) koristeÄi diklorometana kao otapalo, praÄeno kromatografijom stupca na silikagelu (20 g) koristeÄi heksan:etil acetat (7:3) kao eluant; (i) pre-absorption on silica gel (1.5 g) using dichloromethane as solvent, followed by column chromatography on silica gel (20 g) using hexane:ethyl acetate (7:3) as eluent;
(ii) obrnuta faza HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda (70:30) kao eluant; i (ii) reverse phase HPLC on C18 silica, using acetonitrile:water (70:30) as eluent; and
(iii) daljnja obrnuta faza HPLC na C18 silicij dioksidu, koristeÄi acetonitril:metanol:voda (50:10:40) kao eluant; (iii) further reverse phase HPLC on C18 silica, using acetonitrile:methanol:water (50:10:40) as eluent;
radi dobivanja spoja iz naslova kao sasvim bijelog Ävrstog proizvoda, t.t. 90-95 Ā°C. to obtain the title compound as a completely white solid, m.p. 90-95 Ā°C.
Ī“ (CDCl3): 2,23 (m, 2H); 2,56 (t, 1H); 3,84 (br.s, 2H); 7,83 (s, 2H). Ī“ (CDCl 3 ): 2.23 (m, 2H); 2.56 (t, 1H); 3.84 (number s, 2H); 7.83 (s, 2H).
MS (termosprej): M/Z [M+H] 487,3. MS (thermospray): M/Z [M+H] 487.3.
C13H7Cl4F5N4S+H zahtijeva 486,9. C13H7Cl4F5N4S+H requires 486.9.
Primjer 49 Example 49
3-ciano-4-(2,2-diklorocikolopropil)-1-(2,6-dikloro-4-pentafluorotiofenil)pirazol 3-cyano-4-(2,2-dichlorocyclopropyl)-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole
Reakcija je vrÅ”ena koristeÄi postupak iz primjera 48 i 3-ciano-1-(2,6-dikloro-4-pentafluorotiofenil)-4-etenilpirazola (WO-A-97/07102) kao polazni materijal. Sirovo tamno smeÄe ulje je proÄiÅ”Äeno kako slijedi: The reaction was carried out using the procedure of example 48 and 3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)-4-ethenylpyrazole (WO-A-97/07102) as starting material. The crude dark brown oil was purified as follows:
(i) pred-apsorpcija na silikagelu (1,5 g) koristeÄi diklorometan kao otapalo, praÄeno kromatografijom stupca na silikagelu (15 g) koristeÄi heksan:eter:diklorometana (8:1:1) kao eluant; (i) pre-absorption on silica gel (1.5 g) using dichloromethane as solvent, followed by column chromatography on silica gel (15 g) using hexane:ether:dichloromethane (8:1:1) as eluant;
(ii) trituracija rezultirajuÄeg blijedo žutog ulja sa diizopropil eterom, praÄeno filtriranjem i isparavanjem pod sniženim tlakom filtrata radi dobivanja žutog ulja koje je oÄvrsnulo stajanjem; (ii) trituration of the resulting pale yellow oil with diisopropyl ether, followed by filtration and evaporation under reduced pressure of the filtrate to give a yellow oil which solidified on standing;
(iii) obrnuta faza HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda (70:30) kao eluant; (iii) reverse phase HPLC on C18 silica, using acetonitrile:water (70:30) as eluent;
(iv) daljnja obrnuta faza HPLC na C18 silicij dioksidu prethodno ispranom sa heksanom, koristeÄi heksan i zatim diklorometan kao eluant; i (iv) further reverse phase HPLC on C18 silica prewashed with hexane, using hexane and then dichloromethane as eluent; and
(v) otapanje rezultirajuÄeg ulja u metanolu, zatim dodavanje vode u otopinu do zamuÄivanja praÄeno hlaÄenjem; (v) dissolving the resulting oil in methanol, then adding water to the solution until cloudy, followed by cooling;
radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 78-80 Ā°C. to obtain the title compound as a white solid, m.p. 78-80 Ā°C.
Ī“ (CDCl3): 1,87 (t, 1H); 2,20 (m, 1H); 2,85 (m, 1H); 7,53 (s, 1H); 7,93 (s, 2H). Ī“ (CDCl 3 ): 1.87 (t, 1H); 2.20 (m, 1H); 2.85 (m, 1H); 7.53 (s, 1H); 7.93 (s, 2H).
MS (termosprej): M/Z [M+NH4] 489,1. MS (thermospray): M/Z [M+NH 4 ] 489.1.
C13H6Cl4F5N3S+NH4 zahtijeva 488,9. C13H6Cl4F5N3S+NH4 requires 488.9.
Priprema 1 Preparation 1
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-jodopirazol 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodopyrazole
N-jodosukcinimid (3,52 g) dodan je u dijelovima, tokom 5 minuta, u izmijeÅ”anu otopinu 5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-pirazola (EP-A-0295117; 5,0 g) u acetonitrilu (60 ml) na sobnoj temperaturi. Nakon mijeÅ”anja tokom 1 sata, reakcijska smjesa je isparena pod sniženim tlakom radi dobivanja zahtjevanog sirovog proizvoda (8,2 g) koji se, usprkos sadržavanja sukcinimida, može koristiti bez daljnjeg proÄiÅ”Äavanja. N-iodosuccinimide (3.52 g) was added portionwise over 5 minutes to a stirred solution of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole (EP-A-0295117 ; 5.0 g) in acetonitrile (60 ml) at room temperature. After stirring for 1 hour, the reaction mixture was evaporated under reduced pressure to obtain the required crude product (8.2 g) which, despite containing succinimide, could be used without further purification.
Ako se želi, proÄiÅ”Äavanje se može vrÅ”iti dijeljenjem sirovog proizvoda izmeÄu diklorometana i vode, izdvajanjem i suÅ”enjem (MgSO4) organske faze i njegovim isparavanjem pod sniženim tlakom, zatim trituracijom rezultirajuÄeg žutog Ävrstog proizvoda sa heksanom radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 213 Ā°C (razlag.). If desired, purification can be accomplished by partitioning the crude product between dichloromethane and water, separating and drying (MgSO4) the organic phase and evaporating it under reduced pressure, then trituring the resulting yellow solid with hexane to give the title compound as a white solid, m.p. 213 Ā°C (dec.).
Priprema 2 Preparation 2
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-etenilpirazol 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethenylpyrazole
Tri-n-butil(vinil)kositar (4,25 g) i tetrakis(trifenilfosfin)paladij(0) (0,3 g) dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 1 (2,0 g) u dimetilformamidu (10 ml) na sobnoj temperaturi i rezultirajuÄa smjesa je zagrijavana na 75 Ā°C tokom 1 sata, zatim je mijeÅ”ana na sobnoj temperaturi slijedeÄih 60 sati, prije razblaživanja sa vodom. Smjesa je ekstrahirana sa eterom i kombinirani ekstrakti su isprani sa slanom vodom, osuÅ”eni (MgSO4) i ispareni pod sniženim tlakom radi dobivanja sirovog proizvoda (6,0 g) kao crno ulje, koje je proÄiÅ”Äeno kromatografijom stupca na silikagelu (200 g), koristeÄi heksan:diklorometan (1:1) kao eluant, radi dobivanja spoja iz naslova kao Ävrsti proizvod boje kože, t.t. 186-187 Ā°C. Tri-n-butyl(vinyl)tin (4.25 g) and tetrakis(triphenylphosphine)palladium(0) (0.3 g) were added to a stirred solution of the title compound of Preparation 1 (2.0 g) in dimethylformamide (10 ml) at room temperature and the resulting mixture was heated to 75 Ā°C for 1 hour, then stirred at room temperature for a further 60 hours, before dilution with water. The mixture was extracted with ether and the combined extracts were washed with brine, dried (MgSO 4 ) and evaporated under reduced pressure to give the crude product (6.0 g) as a black oil, which was purified by column chromatography on silica gel (200 g) using hexane:dichloromethane (1:1) as eluent, to obtain the title compound as a skin-colored solid, m.p. 186-187 Ā°C.
Ī“ (CDCl3): 3,85 (s, 2H); 5,41 (d, 1H); 5,70 (d, 1H); 6,52 (dd, 1H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 3.85 (s, 2H); 5.41 (d, 1H); 5.70 (d, 1H); 6.52 (dd, 1H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+H] 347,0. MS (thermospray): M/Z [M+H] 347.0.
C13H7Cl2F3N4 +H zahtijeva 347,0. C13H7Cl2F3N4 +H requires 347.0.
Priprema 3 Preparation 3
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-jodopirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodopyrazole
t-butil nitrit (144 ml) dodan je tokom 30 minuta u izmijeÅ”anu otopinu spoja iz naslova pripreme 1 (90 g) u tetrahidrofuranu (720 ml) na 65 Ā°C. Nakon 3 sata na 65 Ā°C, reakcijska smjesa je ostavljena da se ohladi i isparena je pod sniženim tlakom, zatim je talog kristaliziran iz propanola radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 83-84 Ā°C. t-Butyl nitrite (144 ml) was added over 30 minutes to a stirred solution of the compound from the title preparation 1 (90 g) in tetrahydrofuran (720 ml) at 65 Ā°C. After 3 hours at 65 Ā°C, the reaction mixture was allowed to cool and evaporated under reduced pressure, then the precipitate was crystallized from propanol to give the title compound as a white solid, m.p. 83-84 Ā°C.
Ī“ (CDCl3): 7,70 (s, 1H); 7,79 (s, 2H). Ī“ (CDCl 3 ): 7.70 (s, 1H); 7.79 (s, 2H).
MS (termosprej): M/Z [M+NH4] 448,8. MS (thermospray): M/Z [M+NH 4 ] 448.8.
C11H3Cl2F3IN3 +NH4 zahtijeva 448,9. C11H3Cl2F3IN3 +NH4 requires 448.9.
Priprema 4 Preparation 4
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-etenilpirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethenylpyrazole
Otopina spoja iz naslova Pripreme 3 (58 g), tri-n-butil(vinil)kositra (116 ml) i tetrakis(trifenilfosfin)paladija(0) (3,5 g) u dimetilformamidu (350 ml) mijeÅ”an je na 75 Ā°C tokom 3 sata i zatim je ostavljen da se ohladi. Reakcijska smjesa je podijeljena izmeÄu etera (600 ml) i vode (600 ml), zatim je organska faza isprana sukcesivno sa vodom (Ć 5) i slanom vodom, osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom. Kristalizacija taloga iz propan-2-ola dala je spoj iz naslova kao blijedo smeÄi Ävrsti proizvod, t.t. 75-76 Ā°C. A solution of the compound from the title of Preparation 3 (58 g), tri-n-butyl(vinyl)tin (116 ml) and tetrakis(triphenylphosphine)palladium(0) (3.5 g) in dimethylformamide (350 ml) was stirred at 75 Ā° C for 3 hours and then allowed to cool. The reaction mixture was partitioned between ether (600 ml) and water (600 ml), then the organic phase was washed successively with water (Ć5) and brine, dried (Na2SO4) and evaporated under reduced pressure. Crystallization of the precipitate from propan-2-ol gave the title compound as a pale brown solid, m.p. 75-76 Ā°C.
Ī“ (CDCl3): 5,50 (d, 1H); 5,94 (d, 1H); 6,64 (dd, 1H); 7,64 (s,1H); 7,77 (s, 2H). Ī“ (CDCl 3 ): 5.50 (d, 1H); 5.94 (d, 1H); 6.64 (dd, 1H); 7.64 (s, 1H); 7.77 (s, 2H).
MS (termosprej): M/Z [M+NH4] 349,5. MS (thermospray): M/Z [M+NH 4 ] 349.5.
C13H6Cl2F3N3 + NH4 zahtijeva 349,02. C13H6Cl2F3N3 + NH4 requires 349.02.
Priprema 5 Preparation 5
5-amino-3-ciano-1-(2,6-dikloro-4-pentafluorotiofenil)-4-jodopirazol 5-amino-3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)-4-iodopyrazole
N-lodosukcinimid (11,5 g) dodan je u 4 dijela, tokom 5 minuta, u izmijeÅ”anu otopinu 5-amino-3-ciano-1-(2,6-dikloro-4-pentafluorotiofenil)pirazola (WO-A-93/06089; 18,95 g) u acetonitrilu (100 ml) na sobnoj temperaturi. Nakon daljnjih 15 minuta, reakcijska smjesa je isparena pod sniženim tlakom i preostali ostatak je tretiran sa smjesom diklorometana i vode. Netopljivi materijal je sakupljen filtracijom i otopljen u etil acetatu, zatim je ova otopina osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom radi dobivanja spoja iz naslova kao Ävrsti proizvod boje kože, t.t. 253 Ā°C. N-lodosuccinimide (11.5 g) was added in 4 portions over 5 minutes to a stirred solution of 5-amino-3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)pyrazole (WO-A-93 /06089; 18.95 g) in acetonitrile (100 ml) at room temperature. After a further 15 minutes, the reaction mixture was evaporated under reduced pressure and the remaining residue was treated with a mixture of dichloromethane and water. The insoluble material was collected by filtration and dissolved in ethyl acetate, then this solution was dried (Na2SO4) and evaporated under reduced pressure to give the title compound as a skin colored solid, m.p. 253 Ā°C.
Ī“ (CDCl3): 3,94 (br.s, 2H); 7,92 (s, 2H). Ī“ (CDCl 3 ): 3.94 (no.s, 2H); 7.92 (s, 2H).
MS (termosprej): M/Z [M+NH4] 521,9. MS (thermospray): M/Z [M+NH4] 521.9.
C10H4Cl2F5IN4S+NH4 zahtijeva 521,88. C10H4Cl2F5IN4S+NH4 requires 521.88.
Priprema 6 Preparation 6
5-amino-3-ciano-1-(2,6-dikloro-4-pentafluorotiofenil)-4-etenilpirazol 5-amino-3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)-4-ethenylpyrazole
Tri-n-butil(vinil)kositar (4,5 ml) je dodan u izmijeÅ”anu, depliniranu otopinu spoja iz naslova pripreme 5 (5,05 g) i tetrakis(trifenilfosfin)paladija(0) (0,175 g) u dimetilformamidu (32 ml) na sobnoj temperaturi i rezultirajuÄa smjesa je zagrijavana na 70 Ā°C tokom 30 minuta. Nakon daljnjeg 1 sata na 70 Ā°C, tri-n-butil(vinil)kositar (4,5 ml) i tetrakis(trifenilfosfin)paladij(0) (0,175 g) su dodani i reakcijska smjesa je zagrijavana na 70 Ā°C tokom 1 sata, zatim je isparena pod sniženim tlakom. Preostali talog je podijeljen izmeÄu etera i vode, zatim je izdvojena organska faza kombinirana sa ekstraktima etera iz vodene faze, isprana je sa slanom vodom, osuÅ”ena (MgSO4) i isparena pod sniženim tlakom radi dobivanja smeÄe paste koja je triturirana sa heksanom. RezultirajuÄi smeÄi Ävrsti proizvod je tretiran sa etil acetatom, smjesa je filtrirana, filtrat je isparen pod sniženim tlakom i preostali talog je kristaliziran iz toluena radi dobivanja spoja iz naslova kao Ävrsti proizvod boje kože, t.t. 227-228 Ā°C. Tri-n-butyl(vinyl)tin (4.5 mL) was added to a stirred, desaturated solution of the title compound of Preparation 5 (5.05 g) and tetrakis(triphenylphosphine)palladium(0) (0.175 g) in dimethylformamide (32 ml) at room temperature and the resulting mixture was heated to 70 Ā°C for 30 minutes. After a further 1 h at 70 Ā°C, tri-n-butyl(vinyl)tin (4.5 ml) and tetrakis(triphenylphosphine)palladium(0) (0.175 g) were added and the reaction mixture was heated at 70 Ā°C for 1 hour, then evaporated under reduced pressure. The remaining precipitate was partitioned between ether and water, then the separated organic phase was combined with the ether extracts from the aqueous phase, washed with brine, dried (MgSO4) and evaporated under reduced pressure to give a brown paste which was triturated with hexane. The resulting brown solid was treated with ethyl acetate, the mixture was filtered, the filtrate was evaporated under reduced pressure and the remaining precipitate was crystallized from toluene to give the title compound as a skin colored solid, m.p. 227-228 Ā°C.
Ī“ (CDCl3): 3,86 (s, 2H); 5,41 (d, 1H); 5,68 (d, 1H); 6,50 (dd, 1H); 7,92 (s, 2H). Ī“ (CDCl 3 ): 3.86 (s, 2H); 5.41 (d, 1H); 5.68 (d, 1H); 6.50 (dd, 1H); 7.92 (s, 2H).
MS (termosprej): M/Z [M+H] 405,1. MS (thermospray): M/Z [M+H] 405.1.
C12H7Cl2F5N4S+H zahtijeva 404,98. C12H7Cl2F5N4S+H requires 404.98.
Priprema 7 Preparation 7
3-ciano-1-(2,6-dikloro-4-pentafluorotiofenil)-4-jodopirazol 3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)-4-iodopyrazole
Otpina t-butil nitrita (3,1 g) u tetrahidrofuranu (15 ml) dodana je ukapavanjem tokom 30 minuta u izmijeÅ”anu otopinu spoja iz naslova pripreme 5 (2,5 g) u tetrahidrofuranu (35 ml), zatim je reakcijska smjesa isparena pod sniženim tlakom. Kristalizacija preostalog taloga iz propan-2-ola dala je spoj iz naslova kao crvenkasti Ävrsti proizvod, t.t. 179-180 Ā°C. A solution of t-butyl nitrite (3.1 g) in tetrahydrofuran (15 ml) was added dropwise over 30 minutes to a mixed solution of the compound from the title of preparation 5 (2.5 g) in tetrahydrofuran (35 ml), then the reaction mixture was evaporated under reduced pressure. Crystallization of the remaining precipitate from propan-2-ol gave the title compound as a reddish solid, m.p. 179-180 Ā°C.
Ī“ (CDCl3): 7,66 (s, 1H); 7,90 (s, 2H). Ī“ (CDCl 3 ): 7.66 (s, 1H); 7.90 (s, 2H).
MS (termosprej): M/Z [M+NH4] 506,4. MS (thermospray): M/Z [M+NH 4 ] 506.4.
C10H3Cl2F5IN3S+NH4 zahtijeva 506,87. C10H3Cl2F5IN3S+NH4 requires 506.87.
Priprema 8 Preparation 8
3-ciano-1-(2,6-dikloro-4-pentafluorotiofenil)-4-etenilpirazol 3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)-4-ethenylpyrazole
Tri-n-butil(vinil)kositar (4,2 ml) dodan je u izmijeÅ”anu, depliniranu otopinu spoja iz naslova pripreme 7 (1,23 g) i tetrakis(trifenilfosfin)paladija(0) (0,09 g) u dimetilformamidu (32 ml) na sobnoj temperaturi i rezultirajuÄa smjesa je zagrijavana na 70 Ā°C tokom 1,5 sata, prije isparavanja pod sniženim tlakom. Preostali talog je trituriran sa heksanom i rezultirajuÄi Ävrsti proizvod je proÄiÅ”Äen otapanjem u diklorometanu i kromatografijom stupca otopine na silikagelu (60 g), koristeÄi heksan i zatim heksan:diklorometan (80:20) kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 156 Ā°C. Tri-n-butyl(vinyl)tin (4.2 ml) was added to a stirred, desaturated solution of the title compound of Preparation 7 (1.23 g) and tetrakis(triphenylphosphine)palladium(0) (0.09 g) in dimethylformamide (32 ml) at room temperature and the resulting mixture was heated to 70 Ā°C for 1.5 hours, before evaporation under reduced pressure. The remaining precipitate was triturated with hexane and the resulting solid was purified by dissolving in dichloromethane and column chromatography of the solution on silica gel (60 g) using hexane and then hexane:dichloromethane (80:20) as eluent to give the title compound as a white solid , m.p. 156 Ā°C.
Ī“ (CDCl3): 5,50 (d, 1H); 5,95 (d, 1H); 6,63 (dd, 1H); 7,77 (s, 1H); 7,92 (s, 2H). Ī“ (CDCl 3 ): 5.50 (d, 1H); 5.95 (d, 1H); 6.63 (dd, 1H); 7.77 (s, 1H); 7.92 (s, 2H).
MS (termosprej): M/Z [M+NH4] 406,8. MS (thermospray): M/Z [M+NH 4 ] 406.8.
C12H6Cl2F5N3S+NH4 zahtijeva 406,99. C12H6Cl2F5N3S+NH4 requires 406.99.
Priprema 9 Preparation 9
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-formilpirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-formylpyrazole
Otopina spoja iz naslova pripreme 4 (0,1 g), 2,5 mas. % otopina osmij tetroksida u t-butanolu (50 Āµl) i 4-metilmorfolin-N-oksid (0,005 g) u 90 % vodenom acetonu (50 ml) mijeÅ”ana je na sobnoj temperaturi tokom 16 sati. Natrij metaperiodat (0,005 g) je dodan i reakcijska smjesa je mijeÅ”ana daljnjih 16 sati, zatim je isparena pod sniženim tlakom. Preostali talog je podijeljen izmeÄu etera i zasiÄene vodene otopine natrij bikarbonata, vodena faza je izdvojena i ekstrahirana sa eterom, zatim su kombinirani ekstrakti etera osuÅ”eni (Na2SO4) i ispareni pod sniženim tlakom. Preostali talog je proÄiÅ”Äen kromatografijom stupca na silikagelu (5 g), koristeÄi diklorometan kao eluanta, radi dobivanja spoja iz naslova kao žuto-sivi Ävrsti proizvod, t.t. 167,5-168,5 Ā°C. Solution of the compound from the title of preparation 4 (0.1 g), 2.5 wt. % solution of osmium tetroxide in t-butanol (50 Āµl) and 4-methylmorpholine-N-oxide (0.005 g) in 90% aqueous acetone (50 ml) was stirred at room temperature for 16 hours. Sodium metaperiodate (0.005 g) was added and the reaction mixture was stirred for a further 16 h, then evaporated under reduced pressure. The remaining precipitate was partitioned between ether and saturated aqueous sodium bicarbonate, the aqueous phase was separated and extracted with ether, then the combined ether extracts were dried (Na2SO4) and evaporated under reduced pressure. The remaining precipitate was purified by column chromatography on silica gel (5 g), using dichloromethane as eluent, to give the title compound as a yellow-gray solid, m.p. 167.5-168.5 Ā°C.
Ī“ (CDCl3): 7,80 (s, 2H); 8,18 (s, 1H); 10,08 (s, 1H). Ī“ (CDCl 3 ): 7.80 (s, 2H); 8.18 (s, 1H); 10.08 (s, 1H).
MS (termosprej): M/Z [M+NH4] 351,3. MS (thermospray): M/Z [M+NH 4 ] 351.3.
C12H4Cl2F3N3O+NH4 zahtijeva 351,0. C12H4Cl2F3N3O+NH4 requires 351.0.
Priprema 10 Preparation 10
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(2-metilpropen-1-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(2-methylpropen-1-yl)pyrazole
2,5 M otopine n-butillitija u heksanu (0,9 ml) dodana je u izmijeÅ”anu otopinu prop-2-iltrifenilfosfonij jodida (0,97 g) u nevodenom eteru (10 ml) na sobnoj temperaturi radi dobivanja tamno crvene otopine. Otopina spoja iz naslova pripreme 9 (0,6 g) u eteru (20 ml) je dodana i reakcijska smjesa je mijeÅ”ana tokom 2 sata, isprana je sa vodom (20 ml), osuÅ”ena (MgSO4) i isparena pod sniženim tlakom. Preostali talog je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi diklorometan kao eluant, radi dobivanja spoja iz naslova kao blijedi žutosmeÄi Ävrsti proizvod, t.t. 72-74 Ā°C. A 2.5 M solution of n-butyllithium in hexane (0.9 ml) was added to a stirred solution of prop-2-yltriphenylphosphonium iodide (0.97 g) in anhydrous ether (10 ml) at room temperature to give a deep red solution. A solution of the title compound of Preparation 9 (0.6 g) in ether (20 ml) was added and the reaction mixture was stirred for 2 hours, washed with water (20 ml), dried (MgSO4) and evaporated under reduced pressure. The remaining precipitate was purified by column chromatography on silica gel, using dichloromethane as eluent, to afford the title compound as a pale tan solid, m.p. 72-74 Ā°C.
Ī“ (CDCl3): 1,90 (s, 3H); 1,99 (s, 3H); 6,17 (s, 1H); 7,60 (s, 1H); 7,77 (s, 2H). Ī“ (CDCl 3 ): 1.90 (s, 3H); 1.99 (s, 3H); 6.17 (s, 1H); 7.60 (s, 1H); 7.77 (s, 2H).
MS (termosprej): M/Z [M+NH4] 360,2. MS (thermospray): M/Z [M+NH4] 360.2.
C15H10Cl2F3N3 +NH4 zahtijeva 360,03. C15H10Cl2F3N3 +NH4 requires 360.03.
Priprema 11 Preparation 11
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-trimetilsililetinilpirazol 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trimethylsilylethynylpyrazole
Trimetilsililacetilen (3 ml), bakar jodid (150 mg) i bis(trifenilfosfin)paladij(II) klorid (300 mg) dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 1 (6,96 g) u smjesi trietilamina (30 ml) i dimetilformamida (6 ml) na sobnoj temperaturi i rezultirajuÄa smjesa je zagrijavana na 50-60 Ā°C tokom 1 sata. Dodano je joÅ” trimetilsilil acetilena (0,3 ml), zatim je reakcijska smjesa mijeÅ”ana tokom 30 minuta na 50-60 Ā°C, ostavljena da se ohladi i razblažena sa vodom (250 ml). Ova smjesa je ekstrahirana sa eterom (250 ml), koristeÄi slanu vodu da se olakÅ”a izdvajanje faze, i vodena faza je izdvojena i ekstrahirana sa eterom (250 ml). Kombinirani ekstrakti etera su osuÅ”eni (MgSO4) i ispareni pod sniženim tlakom radi dobivanja gume (4,67 g) koja je proÄiÅ”Äena kromatografijom stupca na silikagelu, koristeÄi heksan-diklorometan (1:1) kao eluant, praÄeno kristalizacijom zahtjevanog materijala iz heksan-etera, Äime se dobiva spoj iz naslova kao bijeli Ävrsti proizvod, t.t. 181-182 Ā°C. Trimethylsilylacetylene (3 ml), copper iodide (150 mg) and bis(triphenylphosphine)palladium(II) chloride (300 mg) were added to a mixed solution of the compound from the title preparation 1 (6.96 g) in a mixture of triethylamine (30 ml) and of dimethylformamide (6 ml) at room temperature and the resulting mixture was heated to 50-60 Ā°C for 1 hour. More trimethylsilyl acetylene (0.3 ml) was added, then the reaction mixture was stirred for 30 minutes at 50-60 Ā°C, allowed to cool and diluted with water (250 ml). This mixture was extracted with ether (250 ml), using brine to facilitate phase separation, and the aqueous phase was separated and extracted with ether (250 ml). The combined ether extracts were dried (MgSO4) and evaporated under reduced pressure to give a gum (4.67 g) which was purified by column chromatography on silica gel, using hexane-dichloromethane (1:1) as eluent, followed by crystallization of the required material from hexane-ether , yielding the title compound as a white solid, m.p. 181-182 Ā°C.
Ī“ (CDCl3): 0,20 (s, 9H); 4,10 (br.s, 2H); 7,70 (s, 2H). Ī“ (CDCl 3 ): 0.20 (s, 9H); 4.10 (number s, 2H); 7.70 (s, 2H).
MS (termosprej): M/Z [M+NH4] 434,2. MS (thermospray): M/Z [M+NH 4 ] 434.2.
C16H13Cl2F3N4 Si+NH4 zahtijeva 434,0. C16H13Cl2F3N4 Si+NH4 requires 434.0.
Priprema 12 Preparation 12
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-etinilpirazol 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethynylpyrazole
Kalij karbonat (1,0 g) dodan je u izmijeÅ”anu otopinu spoja iz naslova pripreme 11 (2,0 g) u metanolu (30 ml). Nakon 10 minuta na sobnoj temperaturi, reakcijska smjesa je podijeljena izmeÄu etera (100 ml) i vode (100 ml), zatim je izdvojena organska faza, isprana sa slanom vodom (100 ml), osuÅ”ena (MgSO4) i isparena pod sniženim tlakom. Preostali talog je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi diklorometan kao eluant, praÄeno kristalizacijom iz etera, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 215-216 Ā°C. Potassium carbonate (1.0 g) was added to a stirred solution of the title compound of Preparation 11 (2.0 g) in methanol (30 ml). After 10 min at room temperature, the reaction mixture was partitioned between ether (100 ml) and water (100 ml), then the organic phase was separated, washed with brine (100 ml), dried (MgSO4) and evaporated under reduced pressure. The remaining precipitate was purified by column chromatography on silica gel, using dichloromethane as eluent, followed by crystallization from ether, to give the title compound as a white solid, m.p. 215-216 Ā°C.
Ī“ (CDCl3): 3,49 (s, 1H); 4,20 (br.s, 2H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 3.49 (s, 1H); 4.20 (number s, 2H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+NH4] 362,4. MS (thermospray): M/Z [M+NH 4 ] 362.4.
C13H5Cl2F3N4 +NH4 zahtijeva 362,0. C13H5Cl2F3N4 +NH4 requires 362.0.
Priprema 13 Preparation 13
4-acetil-5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-pirazol 4-acetyl-5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole
P-toluensulfonska kiselina (0,5 g) je dodana u izmijeÅ”anu otopinu spoja iz naslova pripreme 12 (0,345 g) u acetonitrilu (5 ml). Nakon daljnja 2 sata na sobnoj temperaturi, reakcijska smjesa je podijeljena izmeÄu etera (100 ml) i vode (100 ml), zatim je organska faza izdvojena, isprana sukcesivno sa zasiÄenom vodenom otopinom natrij bikarbonata i slanom vodom, osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom. Preostali talog je proÄiÅ”Äen kromatografijom stupca na silikagelu (40 g), koristeÄi heksan:diklorometan (1:10) kao eluanta, radi dobivanja spoja iz naslova kao bijeli kristalni Ävrsti proizvod, t.t. 200-201 Ā°C. P-toluenesulfonic acid (0.5 g) was added to a stirred solution of the title compound of Preparation 12 (0.345 g) in acetonitrile (5 ml). After a further 2 hours at room temperature, the reaction mixture was partitioned between ether (100 ml) and water (100 ml), then the organic phase was separated, washed successively with saturated aqueous sodium bicarbonate solution and brine, dried (Na2SO4) and evaporated under reduced pressure. The remaining precipitate was purified by column chromatography on silica gel (40 g), using hexane:dichloromethane (1:10) as eluent, to give the title compound as a white crystalline solid, m.p. 200-201 Ā°C.
Ī“ (CDCl3): 2,65 (s, 3H); 5,83 (br.s, 2H); 7,82 (s, 2H). Ī“ (CDCl 3 ): 2.65 (s, 3H); 5.83 (no.s, 2H); 7.82 (s, 2H).
MS (termosprej): M/Z [M+NH4] 380,4. MS (thermospray): M/Z [M+NH4] 380.4.
C13H7Cl2F3N4O+NH4 zahtijeva 380,03. C13H7Cl2F3N4O+NH4 requires 380.03.
Priprema 14 Preparation 14
4-acetil-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-pirazol 4-acetyl-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole
T-butil nitrit (0,0262 ml) dodan je ukapavanjem u izmijeÅ”anu otopinu spoja iz naslova pripreme 13 (0,4 g) u tetrahidrofuranu (2 ml). Reakcijska smjesa je zagrijavana pod refluksom tokom 30 minuta i zatim je primijenjena na stupac silikagela (1,0 g). Elucija sa tetrahidrofuranom dala je spoj iz naslova kao bijeli Ävrsti proizvod, t.t. 166-168 Ā°C. t-Butyl nitrite (0.0262 ml) was added dropwise to a stirred solution of the title compound 13 (0.4 g) in tetrahydrofuran (2 ml). The reaction mixture was heated under reflux for 30 min and then applied to a column of silica gel (1.0 g). Elution with tetrahydrofuran gave the title compound as a white solid, m.p. 166-168 Ā°C.
Ī“ (CDCl3): 2,67 (s, 3H); 7,80 (s, 2H); 8,12 (s, 1H). Ī“ (CDCl 3 ): 2.67 (s, 3H); 7.80 (s, 2H); 8.12 (s, 1H).
MS (termosprej): M/Z [M+NH4] 365,0. MS (thermospray): M/Z [M+NH 4 ] 365.0.
C13H6Cl2F3N3O+NH4 zahtijeva 365,02. C13H6Cl2F3N3O+NH4 requires 365.02.
Priprema 15 Preparation 15
3-ciano-1-(2,6-dikloro-4-triflurometilfenil)-4-(1-metiletenil)-pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(1-methylethenyl)-pyrazole
2,5 M otopina n-butillitija u tetrahidrofuranu (0,64 ml) dodana je u izmijeÅ”anu suspenziju metiltrifenilfosfonij bromida (0,565 g) u nevodenom eteru (10 ml) radi dobivanja žute otopine, u koju je dodana otopina spoja iz naslova pripreme 14 (0,5 g) u nevodenom tetrahidrofuranu (10 ml). Reakcijska smjesa je zagrijavana na 30 Ā°C tokom 4 sata, ostavljena da se ohladi i podijeljena izmeÄu etera (100 ml) i zasiÄene vodene otopine natrij bikarbonata (100 ml). Organska faza je izdvojena, osuÅ”ena i isparena pod sniženim tlakom, zatim je preostali talog proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:diklorometan (1:9) kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 129-130 Ā°C. A 2.5 M solution of n-butyllithium in tetrahydrofuran (0.64 ml) was added to a stirred suspension of methyltriphenylphosphonium bromide (0.565 g) in anhydrous ether (10 ml) to give a yellow solution, to which was added a solution of the title compound of preparation 14 ( 0.5 g) in anhydrous tetrahydrofuran (10 ml). The reaction mixture was heated at 30 Ā°C for 4 h, allowed to cool and partitioned between ether (100 mL) and saturated aqueous sodium bicarbonate (100 mL). The organic phase was separated, dried and evaporated under reduced pressure, then the remaining precipitate was purified by column chromatography on silica gel, using hexane:dichloromethane (1:9) as eluent, to give the title compound as a white solid, m.p. 129-130 Ā°C.
Ī“ (CDCl3): 2,16 (s, 3H); 5,29 (s, 1H); 5,80 (s, 1H); 7,59 (s, 1H); 7,88 (s, 2H). Ī“ (CDCl 3 ): 2.16 (s, 3H); 5.29 (s, 1H); 5.80 (s, 1H); 7.59 (s, 1H); 7.88 (s, 2H).
MS (termosprej): M/Z [M+NH4] 362,9. MS (thermospray): M/Z [M+NH 4 ] 362.9.
C14H8Cl2F3N3 +NH4 zahtijeva 363,04. C14H8Cl2F3N3 +NH4 requires 363.04.
Priprema 16 Preparation 16
3-ciano-1-(2,6-dikloro-4-pentafluorotiofenil)-4-(2-jodo-1-metoksietil)pirazol 3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)-4-(2-iodo-1-methoxyethyl)pyrazole
Živin oksid (0,325 g) i jodin (0,381 g) dodani su u izmijeÅ”anu otopinu spoja iz naslova iz pripreme 8 (0,5 g) u metanolu (10 ml), zatim je rezultirajuÄa smjesa zagrijavana pod refluksom tokom 3 sata, ostavljena da se ohladi i isparena pod sniženim tlakom. Preostali talog je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi diklorometan kao eluanta, radi dobivanja spoja iz naslova kao žuti Ävrsti proizvod, t.t. 92-94 Ā°C. Mercuric oxide (0.325 g) and iodine (0.381 g) were added to a stirred solution of the title compound from Preparation 8 (0.5 g) in methanol (10 ml), then the resulting mixture was heated under reflux for 3 h, allowed to cooled and evaporated under reduced pressure. The remaining precipitate was purified by column chromatography on silica gel, using dichloromethane as eluent, to give the title compound as a yellow solid, m.p. 92-94 Ā°C.
Ī“ (CDCl3): 3,46 (s, 3H); 3,54 (m, 2H); 4,49 (t, 1H); 7,70 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 3.46 (s, 3H); 3.54 (m, 2H); 4.49 (t, 1H); 7.70 (s, 1H); 7.78 (s, 2H).
Priprema 17 Preparation 17
3-ciano-1-(2,6-diKloro-4-pentafluorotiofenil)-4-(1-metoksietenil)-pirazol 3-cyano-1-(2,6-dichloro-4-pentafluorothiophenyl)-4-(1-methoxyethenyl)-pyrazole
1,8-diazobiciklo[5,4,0]undek-7-en (0,064 g) dodan je u izmijeÅ”anu otopinu spoja iz naslova pripreme 16 (0,2 g) u toluenu (10 ml). Nakon 18 sati na sobnoj temperaturi, reakcijska smjesa je isparena pod sniženim tlakom i preostali talog je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan i zatim heksan:diklorometan (1:5) kao eluante, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 116-118 Ā°C. 1,8-diazobicyclo[5,4,0]undec-7-ene (0.064 g) was added to a stirred solution of the title compound of Preparation 16 (0.2 g) in toluene (10 ml). After 18 hours at room temperature, the reaction mixture was evaporated under reduced pressure and the remaining precipitate was purified by column chromatography on silica gel, using hexane and then hexane:dichloromethane (1:5) as eluants, to give the title compound as a white solid, m.p. 116-118 Ā°C.
Ī“ (CDCl3): 3,75 (s, 3H); 4,45 (d, 1H); 4,98 (d, 1H); 7,78 (s, 2H+1H). Ī“ (CDCl 3 ): 3.75 (s, 3H); 4.45 (d, 1H); 4.98 (d, 1H); 7.78 (s, 2H+1H).
MS (termosprej): M/Z [M+H] 362,1. MS (thermospray): M/Z [M+H] 362.1.
C14H8Cl2F3N3O+H zahtijeva 362,01. C14H8Cl2F3N3O+H requires 362.01.
Priprema 18 Preparation 18
N-[3-cijano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol-4-ilmetiliden]-N'-(4-metilfenilsulfonil)hidrazin, litij sol N-[3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazol-4-ylmethylidene]-N'-(4-methylphenylsulfonyl)hydrazine, lithium salt
Otopina spoja iz naslova pripreme 9 (0,333 g) i p-toluensulfonilhidrazin (0,186 g) u tetrahidrofuranu mijeÅ”ana je na sobnoj temperaturi tokom 10 minuta i zatim su dodana aktivna 3 Ć molekularna sita (2 tablete, ca. 0,11 g). Smjesa je ohlaÄena na -78 Ā°C pod duÅ”ikom i 2,5 M otopine n-butillitija u heksanu (0,4 ml) je dodano tokom 3 minute. Reakcijska smjesa je ostavljena da se zagrije na sobnu temperaturu, filtrirana je i filtrat je tretiran sa heksanom (40 ml). RezultirajuÄi bijeli talog je sakupljen filtriranjem i osuÅ”en radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod. A solution of the title compound 9 (0.333 g) and p-toluenesulfonylhydrazine (0.186 g) in tetrahydrofuran was stirred at room temperature for 10 minutes and then active 3 Ć molecular sieves (2 tablets, ca. 0.11 g) were added. The mixture was cooled to -78 Ā°C under nitrogen and a 2.5 M solution of n-butyllithium in hexane (0.4 ml) was added over 3 min. The reaction mixture was allowed to warm to room temperature, filtered and the filtrate was treated with hexane (40 ml). The resulting white precipitate was collected by filtration and dried to afford the title compound as a white solid.
Ī“ (DMSO d6): 2,28 (s, 3H); 7,10 (d, 2H); 7,45 (s, 1H); 7,68 (d, 2H); 8,23 (s, 1H); 8,28 (s, 2H). Ī“ (DMSO d 6 ): 2.28 (s, 3H); 7.10 (d, 2H); 7.45 (s, 1H); 7.68 (d, 2H); 8.23 (s, 1H); 8.28 (s, 2H).
MS (termosprej): M/Z [M+H] 507,8. MS (thermospray): M/Z [M+H] 507.8.
C19H11Cl2F3N5O2SLi+H zahtijeva 508,02. C19H11Cl2F3N5O2SLi+H requires 508.02.
Priprema 19 Preparation 19
5-amino-1-(2,6-dikloro-4-trifluorometilfenil)-3-metilpirazol 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-methylpyrazole
3-aminokrotononitril (5,0 g) dodan je u izmijeÅ”anu otopinu 2,6-dikloro-4-trifluorometilfenilhidrazina (15,0 g) u etanolu (100 ml), zatim je rezultirajuÄa otopina tretirana sa koncentriranom sumpornom kiselinom (1,0 ml) radi dobivanja bijelog Ävrstog taloga. Smjesa je zagrijavana pod refluksom tokom 6 sati, ostavljena je da se ohladi i mijeÅ”ana je daljnjih 18 sati na sobnoj temperaturi; ovaj ciklus je ponovljen, zatim je dodano joÅ” koncentrirane sumporne kiseline (4 ml). Reakcijska smjesa je grijana na 60 Ā°C tokom 8 sati, ostavljena je da se ohladi, mijeÅ”ana na sobnoj temperaturi tokom 18 sati i isparena pod sniženim tlakom. RezultirajuÄe naranÄasto ulje je podijeljeno izmeÄu diklorometana (100 ml) i vode (100 ml), zatim je organska faza osuÅ”ena, ostavljena da stoji na sobnoj temperaturi tokom 18 sati i filtrirana radi uklanjanja bijelog Ävrstog proizvoda. Filtrat je isparen pod sniženim tlakom radi dobivanja naranÄastog ulja koje je triturirano sa vruÄim heksanom. Na hlaÄenju, otopina heksana je taložila žuto ulje koje se polako kristaliziralo radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 80-83 Ā°C. 3-Aminocrotononitrile (5.0 g) was added to a stirred solution of 2,6-dichloro-4-trifluoromethylphenylhydrazine (15.0 g) in ethanol (100 ml), then the resulting solution was treated with concentrated sulfuric acid (1.0 ml ) to obtain a white solid precipitate. The mixture was heated under reflux for 6 hours, allowed to cool and stirred for a further 18 hours at room temperature; this cycle was repeated, then more concentrated sulfuric acid (4 ml) was added. The reaction mixture was heated to 60 Ā°C for 8 hours, allowed to cool, stirred at room temperature for 18 hours and evaporated under reduced pressure. The resulting orange oil was partitioned between dichloromethane (100 ml) and water (100 ml), then the organic phase was dried, allowed to stand at room temperature for 18 hours and filtered to remove a white solid. The filtrate was evaporated under reduced pressure to give an orange oil which was triturated with hot hexane. On cooling, the hexane solution precipitated a yellow oil which slowly crystallized to give the title compound as a white solid, m.p. 80-83 Ā°C.
NaÄeno: C 42,73; H 2,62; N 13,58. Found: C 42.73; H 2.62; N 13.58.
C11H8Cl2F3N3 zahtijeva C 42,61; H 2,60; N 13,55 %. C11H8Cl2F3N3 requires C 42.61; H 2.60; N 13.55 %.
Ī“ (CDCl3): 2,25 (s, 3H); 3,48 (br.s, 2H); 5,52 (s, 1H); 7,70 (s, 2H). Ī“ (CDCl 3 ): 2.25 (s, 3H); 3.48 (no.s, 2H); 5.52 (s, 1H); 7.70 (s, 2H).
MS (termosprej): M/Z [M] 310,0. MS (thermospray): M/Z [M] 310.0.
C11H8Cl2F3N3 zahtijeva 310,12. C11H8Cl2F3N3 requires 310.12.
Priprema 20 Preparation 20
5-amino-1-(2,6-dikloro-4-trifluorometilfenil)-4-jodo-3-metilpirazol 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodo-3-methylpyrazole
N-jodosukcinimid (5,5 g) je dodan u izmijeÅ”anu otopinu spoja iz naslova pripreme 19 (9,0 g) u acetonitrilu (200 ml) na sobnoj temperaturi. Reakcijska smjesa je zagrijavana pod refluksom tokom 1 sata, ostavljena je na sobnoj temperaturi tokom 18 sati i zatim isparena pod sniženim tlakom. Preostali talog je ekstrahiran sa vruÄim heksanom a talog dobiven iz otopine hladnog heksana je sakupljen i osuÅ”en radi dobivanja spoja iz naslova kao potpuno bijelog Ävrstog proizvoda, t.t. 116-118 Ā°C. N-iodosuccinimide (5.5 g) was added to a stirred solution of the title compound 19 (9.0 g) in acetonitrile (200 ml) at room temperature. The reaction mixture was heated under reflux for 1 hour, left at room temperature for 18 hours and then evaporated under reduced pressure. The remaining precipitate was extracted with hot hexane and the precipitate obtained from the cold hexane solution was collected and dried to give the title compound as an off-white solid, m.p. 116-118 Ā°C.
Ī“ (CDCl3): 2,24 (s, 3H); 3,68 (br.s, 2H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 2.24 (s, 3H); 3.68 (no.s, 2H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+H] 435,8. MS (thermospray): M/Z [M+H] 435.8.
C11 H7 Cl2 F3 IN3+ H zahtijeva 435,91. C11 H7 Cl2 F3 IN3+ H requires 435.91.
Priprema 21 Preparation 21
1-(2,6-dikloro-4-trifluorometilfenil)-4-jodo-3-metilpirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodo-3-methylpyrazole
t-butil nitrit (2,33 ml) dodan je ukapavanjem u izmijeÅ”anu otopinu spoja iz naslova pripreme 20 (2,85 g) u tetrahidrofuranu (35 ml) na 0 Ā°C. Reakcijska smjesa je ostavljena da se zagrije na sobnu temperaturu, zagrijavana je pod refluksom tokom 1,5 sata, zatim je isparena pod sniženim tlakom. Preostali talog je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:diklorometan (1:1) kao eluant, radi dobivanja žutog ulja koje je dalje proÄiÅ”Äeno na sliÄan naÄin, koristeÄi heksan:diklorometan (2:1) kao eluant. Tako je dobiven spoj iz naslova kao bijeli Ävrsti proizvod, t.t. 118,5-119,4 Ā°C. t-Butyl nitrite (2.33 ml) was added dropwise to a stirred solution of the title compound 20 (2.85 g) in tetrahydrofuran (35 ml) at 0 Ā°C. The reaction mixture was allowed to warm to room temperature, heated under reflux for 1.5 hours, then evaporated under reduced pressure. The remaining residue was purified by column chromatography on silica gel, using hexane:dichloromethane (1:1) as eluent, to give a yellow oil which was further purified in a similar manner, using hexane:dichloromethane (2:1) as eluent. The title compound was thus obtained as a white solid, m.p. 118.5-119.4 Ā°C.
Ī“ (CDCL3): 2,18 (s, 3H); 7,54 (s, 1H); 7,70 (s, 2H). Ī“ (CDCl 3 ): 2.18 (s, 3H); 7.54 (s, 1H); 7.70 (s, 2H).
MS (termosprej): M/Z [M+H] 420,5. MS (thermospray): M/Z [M+H] 420.5.
C11H6Cl2F3IN2 +H zahtijeva 420,90. C11H6Cl2F3IN2 +H requires 420.90.
Priprema 22 Preparation 22
1-(2,6-dikloro-4-trifluorometilfenil)-4-etenil-3-metilpirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethenyl-3-methylpyrazole
Tetrakis(trifenilfosfin)paladij(0) (0,1 g) i tri-n-butil(vinil)kositar (2 ml) dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 21 (2,06 g) u dimetilformamidu (25 ml) i reakcijska smjesa je grijana na 70 Ā°C tokom 2 sata, zatim je isparena pod sniženim tlakom. Ostatak je podijeljen izmeÄu etera i vode, vodena faza je izdvojena i ekstrahirana sa eterom (Ć 2) i kombinirane organske otopine su isprane sa slanom vodom, osuÅ”ene (Na2SO4) i isparene pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:eter (9:1) kao eluant, praÄeno obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:voda:metanol (40:50:10) kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 68,1-68,7 Ā°C. Tetrakis(triphenylphosphine)palladium(0) (0.1 g) and tri-n-butyl(vinyl)tin (2 ml) were added to a stirred solution of the title compound of Preparation 21 (2.06 g) in dimethylformamide (25 ml). and the reaction mixture was heated at 70 Ā°C for 2 hours, then evaporated under reduced pressure. The residue was partitioned between ether and water, the aqueous phase was separated and extracted with ether (Ć2) and the combined organic solutions were washed with brine, dried (Na 2 SO 4 ) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using hexane:ether (9:1) as eluent, followed by reverse phase HPLC on C18 silica, using acetonitrile:water:methanol (40:50:10) as eluent, to give the title compound as a white solid, m.p. 68.1-68.7 Ā°C.
Ī“ (CDCl3): 2,44 (s, 3H); 5,24 (d, 1H); 5,50 (d, 1H); 6,62 (dd, 1H); 7,57 (s, 1H); 7,74 (s, 2H). Ī“ (CDCl 3 ): 2.44 (s, 3H); 5.24 (d, 1H); 5.50 (d, 1H); 6.62 (dd, 1H); 7.57 (s, 1H); 7.74 (s, 2H).
MS (termosprej): M/Z [M+H] 321,1. MS (thermospray): M/Z [M+H] 321.1.
C13H9Cl2F3N2 +H zahtijeva 321,02. C13H9Cl2F3N2 +H requires 321.02.
Priprema 23 Preparation 23
1-(2,6-dikloro-4-trifluorometilfenil)-3,5-dimetilpirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-3,5-dimethylpyrazole
Pentan-2,4-dion (0,100 g) je dodan u izmijeÅ”anu otopinu 2,6-dikloro-4-trifluorometilfenilhidrazina (0,245 g) u etanolu (4,5 ml), praÄeno ledenom octenom kiselinom (0,5 ml), na sobnoj temperaturi. Reakcijska smjesa je zagrijavana pod refluksom tokom 1 sata, zatim je isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi diklorometan kao eluant, radi dobivanja bezbojnog ulja koje je poÄetno kristaliziralo, nakon uklanjanja nebitnog otapala u vakuumu, radi dobivanja spoja iz naslova (0,265 g), t.t. 87-89 Ā°C. Pentane-2,4-dione (0.100 g) was added to a stirred solution of 2,6-dichloro-4-trifluoromethylphenylhydrazine (0.245 g) in ethanol (4.5 mL), followed by glacial acetic acid (0.5 mL), at room temperature. The reaction mixture was heated under reflux for 1 hour, then evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using dichloromethane as eluent, to give a colorless oil which initially crystallized, after removal of the essential solvent in vacuo, to give the title compound (0.265 g), m.p. 87-89 Ā°C.
Ī“ (CDCl3): 2,10 (s, 3H); 2,32 (s, 3H); 6,07 (s, 1H); 7,72 (s, 2H). Ī“ (CDCl 3 ): 2.10 (s, 3H); 2.32 (s, 3H); 6.07 (s, 1H); 7.72 (s, 2H).
MS (termosprej): M/Z [M] 309,0. MS (thermospray): M/Z [M] 309.0.
C12H9Cl2F3N2 zahtijeva 309,12. C12H9Cl2F3N2 requires 309.12.
Priprema 24 Preparation 24
1-(2,6-dikloro-4-trifluorometilfenil)-3,5-dimetil-4-jodopirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-3,5-dimethyl-4-iodopyrazole
Otopina N-jodosukcinimida (0,158 g) u acetonitrilu (3 ml) dodana je ukapavanjem u izmijeÅ”anu otopinu spoja iz naslova pripreme 23 (0,218 g) u acetonitrilu (3 ml) na sobnoj temperaturi. Nakon daljnjih 27 sati, reakcijska smjesa je isparena pod sniženim tlakom i ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (5 g) koristeÄi diklorometan kao eluant, radi dobivanja spoja iz naslova kao žuto ulje. A solution of N-iodosuccinimide (0.158 g) in acetonitrile (3 ml) was added dropwise to a stirred solution of the title compound 23 (0.218 g) in acetonitrile (3 ml) at room temperature. After a further 27 hours, the reaction mixture was evaporated under reduced pressure and the residue was purified by column chromatography on silica gel (5 g) using dichloromethane as eluent to afford the title compound as a yellow oil.
Ī“ (CDCl3): 2,11 (s, 3H), 2,32 (s, 3H); 7,73 (s, 2H). Ī“ (CDCl 3 ): 2.11 (s, 3H), 2.32 (s, 3H); 7.73 (s, 2H).
MS (termosprej): M/Z [M+H] 435,0. MS (thermospray): M/Z [M+H] 435.0.
C12H8Cl2F3IN2 +H zahtijeva 434,91. C12H8Cl2F3IN2 +H requires 434.91.
Priprema 25 Preparation 25
1-(2,6-dikloro-4-trifluorometilfenil)-3,5-dimetil-4-etenilpirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-3,5-dimethyl-4-ethenylpyrazole
Otopina spoja iz naslova pripreme 24 (1,0 g), tri-n-butil(vinil)kositar (2 ml) i tetrakis(trifenilfosfin)paladij(0) (0,1 g) u dimetilformamidu (10 ml) mijeÅ”ana je na 75 Ā°C tokom 2 sata i zatim na sobnoj temperaturi tokom 18 sati. Reakcijska smjesa je sekvencijalno mijeÅ”ana na 75 Ā°C tokom 2 sata, tretirana sa tri-n-butil(vinil)kositrom (2 ml), mijeÅ”ana na 75 Ā°C tokom 2 sata, tretirana sa tetrakis(trifenilfosfin)paladijom(0) (0,1 g), mijeÅ”ana na 75 Ā°C tokom 2 sata i isparena pod sniženim tlakom. Ostatak je podijeljen izmeÄu diklorometana i vode, zatim je organska faza izdvojena, isprana sukcesivno sa vodom (Ć 2) i slanom vodom, osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom. RezultirajuÄi sirovi proizvod je apsorbiran na silikagelu (20 g) i zatim proÄiÅ”Äen kromatografijom stupca na silikagelu (150 g), koristeÄi gradijent elucije heksan:diklorometan (100:0 do 0:100), radi dobivanja spoja iz naslova kao žuto ulje. A solution of the compound from the title preparation 24 (1.0 g), tri-n-butyl(vinyl)tin (2 ml) and tetrakis(triphenylphosphine)palladium(0) (0.1 g) in dimethylformamide (10 ml) was mixed at 75 Ā°C for 2 hours and then at room temperature for 18 hours. The reaction mixture was sequentially stirred at 75 Ā°C for 2 h, treated with tri-n-butyl(vinyl)tin (2 ml), stirred at 75 Ā°C for 2 h, treated with tetrakis(triphenylphosphine)palladium(0) (0 ,1 g), stirred at 75 Ā°C for 2 hours and evaporated under reduced pressure. The residue was partitioned between dichloromethane and water, then the organic phase was separated, washed successively with water (Ć 2) and brine, dried (Na2SO4) and evaporated under reduced pressure. The resulting crude product was absorbed on silica gel (20 g) and then purified by column chromatography on silica gel (150 g), using a gradient elution of hexane:dichloromethane (100:0 to 0:100), to afford the title compound as a yellow oil.
Ī“ (CDCl3): 2,11 (s, 3H); 2,40 (s, 3H); 5,23 (d, 1H); 5,41 (d, 1H); 6,59 (dd, 1H); 7,71 (s, 2H). Ī“ (CDCl 3 ): 2.11 (s, 3H); 2.40 (s, 3H); 5.23 (d, 1H); 5.41 (d, 1H); 6.59 (dd, 1H); 7.71 (s, 2H).
MS (termosprej): M/Z [M+H] 335,1. MS (thermospray): M/Z [M+H] 335.1.
C14H11Cl2F3N2 +H zahtijeva 335,03. C14H11Cl2F3N2 +H requires 335.03.
Priprema 26 Preparation 26
5-amino-4-jodo-3-metil-1-(2,4,6-trihlorofenil)pirazol 5-amino-4-iodo-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole
IzmijeÅ”ana otopina 5-amino-3-metil-1-(2,4,6-triklorofenil)pirazola (WO-A-94/13643; 35 g) i N-jodosukcinimida (29 g) u acetonitrilu (450 ml) grijana je pod refluksom tokom 1,5 sata, zatim je reakcijska smjesa ostavljena da se ohladi i isparena je pod sniženim tlakom. Ostatak je otopljen u diklorometanu i otopina je isprana uzastopno sa vodenom otopinom natrij tiosulfata, vodom i slanom vodom, zatim je osuÅ”ena (Na2SO4) i isparena pod sniženim tlakom. RezultirajuÄi tamno obojen Ävrsti proizvod je trituriran sa heksanom radi dobivanja spoja iz naslova kao blijedo naranÄasti Ävrsti proizvod, t.t. 135-137 Ā°C. A mixed solution of 5-amino-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole (WO-A-94/13643; 35 g) and N-iodosuccinimide (29 g) in acetonitrile (450 ml) was heated under reflux for 1.5 hours, then the reaction mixture was allowed to cool and evaporated under reduced pressure. The residue was dissolved in dichloromethane and the solution was washed successively with aqueous sodium thiosulfate, water and brine, then dried (Na2SO4) and evaporated under reduced pressure. The resulting dark colored solid was triturated with hexane to afford the title compound as a pale orange solid, m.p. 135-137 Ā°C.
Ī“ (CDCl3): 2,25 (s, 3H); 3,67 (br.s, 2H); 7,49 (s, 2H). Ī“ (CDCl 3 ): 2.25 (s, 3H); 3.67 (no.s, 2H); 7.49 (s, 2H).
MS (termosprej): M/Z [M+H] 401,4. MS (thermospray): M/Z [M+H] 401.4.
C10H7Cl3IN3+ H zahtijeva 401,88 C10H7Cl3IN3+ H requires 401.88
Priprema 27 Preparation 27
4-jodo-3-metil-1(2,4,6-triklorofenil)pirazol 4-iodo-3-methyl-1(2,4,6-trichlorophenyl)pyrazole
Otopina t-butil nitrita (12 ml) u nevodenom tetrahidrofuranu (50 ml) je dodana ukapavanjem u izmijeŔanu, blago refluksiranu otopinu spoja iz naslova pripreme 26 (18,11 g) u nevodenom tetrahidrofuranu (120 ml). A solution of t-butyl nitrite (12 ml) in anhydrous tetrahydrofuran (50 ml) was added dropwise to a stirred, slightly refluxed solution of the title compound of Preparation 26 (18.11 g) in anhydrous tetrahydrofuran (120 ml).
Reakcijska smjesa je ostavljena da se ohladi i ispari pod sniženim tlakom, zatim je ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan praÄeno sa heksan:etil acetatom (19:1) kao eluanta, radi dobivanja spoja iz naslova kao naranÄasti Ävrsti proizvod, t.t. 97-99 Ā°C. The reaction mixture was allowed to cool and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel, using hexane followed by hexane:ethyl acetate (19:1) as eluent, to give the title compound as an orange solid, m.p. 97-99 Ā°C.
Ī“ (CDCl3): 2,36 (s, 3H); 7,47 (s, 2H); 7,48 (s, 1H). Ī“ (CDCl 3 ): 2.36 (s, 3H); 7.47 (s, 2H); 7.48 (s, 1H).
MS (termosprej): M/Z [M+H] 386,9. MS (thermospray): M/Z [M+H] 386.9.
C10H6Cl3IN2 +H zahtijeva 386,87. C10H6Cl3IN2 +H requires 386.87.
Priprema 28 Preparation 28
4-etenil-3-metil-1-(2,4,6-triklorofenil)pirazol 4-ethenyl-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole
IzmijeÅ”ana otopina spoja iz naslova pripreme 27 (16,62 g), tri-n-butil(vinil)kositra (27,27 g) i tetrakis(trifenilfosfin)paladija(0) (0,6 g) u nevodenom dimetilformamidu (100 ml) zagrijavan je na 75 Ā°C tokom 2,5 sata. Dodano je joÅ” tetrakis(trifenilfosfin)paladija(0) (0,6 g) i reakcijska smjesa je grijana na 75 Ā°C tokom daljnja 2 sata, zatim je isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan i zatim heksan:etil acetat (99:1) kao eluante, radi dobivanja spoja iz naslova kao blijedo žuti Ävrsti proizvod, t.t. 71-73 Ā°C. A mixed solution of the compound from the title preparation 27 (16.62 g), tri-n-butyl(vinyl)tin (27.27 g) and tetrakis(triphenylphosphine)palladium(0) (0.6 g) in anhydrous dimethylformamide (100 ml ) was heated to 75 Ā°C for 2.5 hours. More tetrakis(triphenylphosphine)palladium(0) (0.6 g) was added and the reaction mixture was heated at 75 Ā°C for a further 2 hours, then evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using hexane and then hexane:ethyl acetate (99:1) as eluants, to afford the title compound as a pale yellow solid, m.p. 71-73 Ā°C.
Ī“ (CDCl3): 2,40 (s, 3H); 5,19 (d, 1H); 5,49 (d, 1H); 6,59 (dd, 1H); 7,47 (s, 2H); 7,50 (s, 1H). Ī“ (CDCl 3 ): 2.40 (s, 3H); 5.19 (d, 1H); 5.49 (d, 1H); 6.59 (dd, 1H); 7.47 (s, 2H); 7.50 (s, 1H).
MS (termosprej): M/Z [M+NH4] 287,0. MS (thermospray): M/Z [M+NH 4 ] 287.0.
C12H9Cl3N2 +NH4 zahtijeva 286,99. C12H9Cl3N2 +NH4 requires 286.99.
Priprema 29 Preparation 29
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-trifluoroacetilpirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoroacetylpyrazole
T-butil nitrit (12,45 ml) dodan je ukapavanjem u izmijeÅ”anu otopinu 5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-trifluoroacetilpirazola (JP-A-8-311036; 30 g) u tetrahidrofuranu (250 ml) i smjesa je mijeÅ”ana na 55 Ā°C tokom 16 sati. Daljnje koliÄine t-butil nitrita su dodane/slijedeÄi periodi mijeÅ”anja na 55 Ā°C su bili kako slijedi: 9 ml/7 sati, 6 ml/16 sati, 9 ml/6 sati, 4,75 ml/16 sati, 6 ml/6 sati i 3,5 ml/22 sata. Reakcijska smjesa je ostavljena da se hladi i isparena je pod sniženim tlakom, zatim je ostatak kombiniran sa onim dobivenim iz 3 jednakih priprema. ProÄiÅ”Äavanje kromatografijom stupca na silikagelu (1 kg), koristeÄi heksan:diklorometan (6:4) i zatim diklorometan kao eluanta, dalo je žuto ulje, koje je trituracijom sa heksanom (3 Ć 50 ml) praÄeno diklorometanom (100 ml), dalo spoj iz naslova kao bijeli Ävrsti proizvod, t.t. 124-125 Ā°C. t-Butyl nitrite (12.45 ml) was added dropwise to the stirred solution of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoroacetylpyrazole (JP-A-8-311036; 30 g) in tetrahydrofuran (250 ml) and the mixture was stirred at 55 Ā°C for 16 hours. Further amounts of t-butyl nitrite were added/following stirring periods at 55 Ā°C were as follows: 9 ml/7 hours, 6 ml/16 hours, 9 ml/6 hours, 4.75 ml/16 hours, 6 ml/ 6 hours and 3.5 ml/22 hours. The reaction mixture was allowed to cool and was evaporated under reduced pressure, then the residue was combined with that obtained from 3 equal preparations. Purification by column chromatography on silica gel (1 kg), using hexane:dichloromethane (6:4) and then dichloromethane as eluent, gave a yellow oil, which trituration with hexane (3 x 50 ml) followed by dichloromethane (100 ml) gave the compound from the title as a white solid, m.p. 124-125 Ā°C.
Ī“ (CDCl3): 7,83 (s, 2H); 8,30 (s, 1H). Ī“ (CDCl 3 ): 7.83 (s, 2H); 8.30 (s, 1H).
MS (termosprej): M/Z [M+H] 401,7. MS (thermospray): M/Z [M+H] 401.7.
C13H3Cl2F6N3O+H zahtijeva 401,96. C13H3Cl2F6N3O+H requires 401.96.
Priprema 30 Preparation 30
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(3,3,3-trifluoropropen-2-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3,3,3-trifluoropropen-2-yl)pyrazole
2,5 M otopina n-butillitija u heksanu (0,11 ml) dodana je ukapavanjem u izmijeÅ”anu suspenziju metiltrifenilfosfonij jodida (111 mg) u tetrahidrofuranu (6 ml) pod duÅ”ikom na sobnoj temperaturi. RezultirajuÄa crvenkasto smeÄa otopina je dodana ukapavanjem, pod duÅ”ikom, u izmijeÅ”anu otopinu spoja iz naslova pripreme 29 (100 mg) u tetrahidrofuranu (1 ml) na sobnoj temperaturi i reakcijska smjesa je mijeÅ”ana tokom 30 minuta. Voda (30 ml) je zatim dodana, ekstrakcija sa eterom (50 ml) je izvrÅ”ena i organski ekstrakt je osuÅ”en (Na2SO4) i isparen pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (10 g), koristeÄi heksan:diklorometan (1:1) kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 103-104 Ā°C. A 2.5 M solution of n-butyllithium in hexane (0.11 ml) was added dropwise to a stirred suspension of methyltriphenylphosphonium iodide (111 mg) in tetrahydrofuran (6 ml) under nitrogen at room temperature. The resulting reddish brown solution was added dropwise, under nitrogen, to a stirred solution of the title compound 29 (100 mg) in tetrahydrofuran (1 ml) at room temperature and the reaction mixture was stirred for 30 min. Water (30 ml) was then added, extraction with ether (50 ml) was carried out and the organic extract was dried (Na 2 SO 4 ) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (10 g), using hexane:dichloromethane (1:1) as eluent, to give the title compound as a white solid, m.p. 103-104 Ā°C.
Ī“ (CDCl3): 6,20 (s, 1H); 6,39 (s, 1H); 7,78 (s, 1H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 6.20 (s, 1H); 6.39 (s, 1H); 7.78 (s, 1H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+H] 399,8. MS (thermospray): M/Z [M+H] 399.8.
C14H5Cl2F6N3 +H zahtijeva 400,0. C14H5Cl2F6N3 +H requires 400.0.
Priprema 31 Preparation 31
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(3-trifluorometil-1-pirazolin-3-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3-trifluoromethyl-1-pyrazolin-3-yl)pyrazole
Otopina diazometana (40 mmol) u eteru dodana je polako u izmijeÅ”anu otopinu spoja iz naslova pripreme 30 (27 g) u eteru (150 ml) na sobnoj temperaturi i reakcijska smjesa je mijeÅ”ana tokom 40 minuta. Dodano je polako joÅ” diazometana (50 mmol) u eteru (150 ml) i reakcijska smjesa je mijeÅ”ana tokom daljnjih 16 sati na sobnoj temperaturi. ViÅ”ak diazometana je destiliziran, zatim je otapalo ispareno pod sniženim tlakom radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod. A solution of diazomethane (40 mmol) in ether was added slowly to a stirred solution of the title compound 30 (27 g) in ether (150 ml) at room temperature and the reaction mixture was stirred for 40 minutes. More diazomethane (50 mmol) in ether (150 ml) was added slowly and the reaction mixture was stirred for a further 16 hours at room temperature. Excess diazomethane was distilled off, then the solvent was evaporated under reduced pressure to give the title compound as a white solid.
Ī“ (CDCl3): 2,23 (m, 1H); 2,52 (m, 1H); 4,90 (m, 2H); 7,78 (s, 2H); 8,15 (s, 1H). Ī“ (CDCl 3 ): 2.23 (m, 1H); 2.52 (m, 1H); 4.90 (m, 2H); 7.78 (s, 2H); 8.15 (s, 1H).
MS (termosprej): M/Z [M+NH4] 458,8. MS (thermospray): M/Z [M+NH 4 ] 458.8.
C15H7Cl2F6N5 +NH4 zahtijeva 459,0. C15H7Cl2F6N5 +NH4 requires 459.0.
Priprema 32 Preparation 32
5-kloro-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-jodopirazol 5-chloro-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodopyrazole
Ca. 1M otopine nitrozil klorida u diklorometanu (2,7 ml) dodano je ukapavanjem u izmijeÅ”anu, ledom-ohlaÄenu otopinu spoja iz naslova pripreme 1 (1,0 g) u acetonitrilu (15 ml), zatim je reakcijska smjesa grijana pod refluksom tokom 10 minuta i isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:toluen (2:1) i zatim toluena kao eluanta, radi dobivanja spoja iz naslova kao blijedo naranÄasti Ävrsti proizvod, t.t. 115,7-116,3 Ā°C. What. A 1M solution of nitrosyl chloride in dichloromethane (2.7 ml) was added dropwise to a stirred, ice-cooled solution of the title compound 1 (1.0 g) in acetonitrile (15 ml), then the reaction mixture was heated under reflux for 10 minutes and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using hexane:toluene (2:1) and then toluene as eluent, to afford the title compound as a pale orange solid, m.p. 115.7-116.3 Ā°C.
Ī“ (CDCl3): 7,80 (s, 2H). Ī“ (CDCl 3 ): 7.80 (s, 2H).
MS (termosprej): M/Z [M+H] 466,0. MS (thermospray): M/Z [M+H] 466.0.
C11H2Cl3F3IN3 +H zahtijeva 465,84. C11H2Cl3F3IN3 +H requires 465.84.
Priprema 33 Preparation 33
5-kloro-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-etenilpirazol 5-chloro-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethenylpyrazole
Tetrakis(trifenilfosfin)paladij(0) (0,448 g) dodan je u izmijeÅ”anu otopinu spoja iz naslova pripreme 32 (6,0 g) u dimetilformamidu (75 ml) na sobnoj temperaturi praÄeno, 5 minuta kasnije, dodavanjem ukapavanjem tri-n-butil(vinil)kositra (11,3 ml). RezultirajuÄa smjesa je grijana na 70 Ā°C tokom 18 sati, zatim je isparena pod sniženim tlakom i ostatak je podijeljen izmeÄu etera i vode. Organska faza je izdvojena, osuÅ”ena i isparena pod sniženim tlakom, zatim je rezultirajuÄi ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan i zatim heksan:diklorometan (2:1) kao eluant, praÄeno kristalizacijom iz heksana, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 69,8-70,4 Ā°C. Tetrakis(triphenylphosphine)palladium(0) (0.448 g) was added to a stirred solution of the title compound of Preparation 32 (6.0 g) in dimethylformamide (75 mL) at room temperature followed, 5 min later, by the dropwise addition of tri-n-butyl (vinyl) tin (11.3 ml). The resulting mixture was heated at 70 Ā°C for 18 hours, then evaporated under reduced pressure and the residue partitioned between ether and water. The organic phase was separated, dried and evaporated under reduced pressure, then the resulting residue was purified by column chromatography on silica gel using hexane and then hexane:dichloromethane (2:1) as eluent, followed by crystallization from hexane to give the title compound as a white solid product, m.p. 69.8-70.4 Ā°C.
Ī“ (CDCl3): 5,61 (d, 1H); 6,20 (d, 1H); 6,56 (dd, 1H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 5.61 (d, 1H); 6.20 (d, 1H); 6.56 (dd, 1H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+NH4] 383,1. MS (thermospray): M/Z [M+NH 4 ] 383.1.
C13H5Cl3F3N3+NH4 zahtijeva 382,98. C13H5Cl3F3N3+NH4 requires 382.98.
Priprema 34 Preparation 34
5-amino-1-(2,6-dikloro-4-trifluorometilfenil)-4-jodo-3-trifluorometilpirazol 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodo-3-trifluoromethylpyrazole
Dobiven je iz 5-amino-1-(2,6-dikloro-4-trifluorometilfenil)-3-trifluorometilpirazola (WO-A-87/03781), analogno sa pripremom 1, kao potpuno bijeli Ävrsti proizvod, t.t. 126 Ā°C. It was obtained from 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole (WO-A-87/03781), analogously to preparation 1, as an off-white solid product, m.p. 126 Ā°C.
Ī“ (CDCl3): 3,90 (br.s, 2H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 3.90 (no.s, 2H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+H] 490,2. MS (thermospray): M/Z [M+H] 490.2.
C11H4Cl2F6IN3 +H zahtijeva 489,88. C11H4Cl2F6IN3 +H requires 489.88.
Priprema 35 Preparation 35
1-(2,6-dikloro-4-trifluorometilfenil)-4-jodo-3-trifluorometilpirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodo-3-trifluoromethylpyrazole
Dobiven je iz spoja iz naslova pripreme 34, analogno sa pripremom 3, kao ulje koje je oÄvrsnulo stajanjem. Kristalizacija iz propan-2-ola dala je spoj iz naslova kao žuti Ävrst proizvod, t.t. 109-112 Ā°C. It was obtained from the compound from the title of preparation 34, analogously to preparation 3, as an oil which solidified on standing. Crystallization from propan-2-ol gave the title compound as a yellow solid, m.p. 109-112 Ā°C.
NaÄeno: C 27,87; H 0,69; H 6,15. Found: C 27.87; H 0.69; H 6.15.
C11H4Cl2F6IN3 zahtijeva C 27,82; H 0,64; N 5,90 %. C11H4Cl2F6IN3 requires C 27.82; H 0.64; N 5.90 %.
Ī“ (CDCl3): 7,70 (s, 1H); 7,77 (s, 2H). Ī“ (CDCl 3 ): 7.70 (s, 1H); 7.77 (s, 2H).
Priprema 36 Preparation 36
1-(2,6-dikloro-4-trifluorometilfenil)-4-etenil-3-trifluorometilpirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethenyl-3-trifluoromethylpyrazole
Dobiven je iz spoja iz naslova pripreme 35, analogno sa pripremom 4, osim Å”to je sirovi proizvod kristaliziran iz heksana i zatim je dalje proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi eter kao eluant, praÄeno obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:metanol:vodu (40:10:50) kao eluant, praÄeno kristalizacijom iz propan-2-ola, radi dobivanja spoja iz naslova kao blijedo žuti Ävrsti proizvod, t.t. 95-98 Ā°C. It was obtained from the title compound of Preparation 35, analogously to Preparation 4, except that the crude product was crystallized from hexane and then further purified by column chromatography on silica gel, using ether as eluent, followed by reverse phase HPLC on C18 silica, using acetonitrile:methanol :water (40:10:50) as eluent, followed by crystallization from propan-2-ol to afford the title compound as a pale yellow solid, m.p. 95-98 Ā°C.
Ī“ (CDCl3): 5,39 (d, 1H); 5,65 (d, 1H); 6,69 (dd, 1H); 7,80 (s, 1H); 7,81 (s, 2H). Ī“ (CDCl 3 ): 5.39 (d, 1H); 5.65 (d, 1H); 6.69 (dd, 1H); 7.80 (s, 1H); 7.81 (s, 2H).
MS (termosprej): M/Z [M+NH4] 391,9. MS (thermospray): M/Z [M+NH4] 391.9.
C13H6Cl2F6N2 + NH4 zahtijeva 392,02. C13H6Cl2F6N2 + NH4 requires 392.02.
Priprema 37 Preparation 37
5-amino-1-(2,6-dikloro-4-trifluorometilfenil)-3-fenilpirazol 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-phenylpyrazole
Otopina 2,6-dikloro-4-trifluorometilfenilhidrazina (0,245 g) u etanolu (2 ml) dodana je u izmijeÅ”anu otopinu benzoacetonitrila (0,145 g) u etanolu (8 ml) i rezultirajuÄa otopina je grijana pod refluksom tokom 6 sati. Ledena octena kiselina (1 ml) je dodana i rezultirajuÄa smjesa je grijana pod refluksom tokom daljnjih 6 sati i zatim je isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (10 g), koristeÄi diklorometan kao eluant, praÄeno obrnutom fazom HPLC na C18 silicij dioksidu, koristeÄi acetonitril:metanol:vodu (50:10:40) kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrst proizvod, t.t. 141,5-142,5 Ā°C. A solution of 2,6-dichloro-4-trifluoromethylphenylhydrazine (0.245 g) in ethanol (2 ml) was added to a stirred solution of benzoacetonitrile (0.145 g) in ethanol (8 ml) and the resulting solution was heated under reflux for 6 hours. Glacial acetic acid (1 ml) was added and the resulting mixture was heated under reflux for a further 6 hours and then evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (10 g), using dichloromethane as eluent, followed by reverse phase HPLC on C18 silica, using acetonitrile:methanol:water (50:10:40) as eluent, to give the title compound as a white solid product, m.p. 141.5-142.5 Ā°C.
Ī“ (CDCl3): 3,60 (br.s, 2H); 6,08 (s, 1H); 7,30-7,45 (m, 3H); 7,80 (s, 2H); 7,80-7,85 (m, 2H). Ī“ (CDCl 3 ): 3.60 (no.s, 2H); 6.08 (s, 1H); 7.30-7.45 (m, 3H); 7.80 (s, 2H); 7.80-7.85 (m, 2H).
MS (termosprej): M/Z [M+H] 372,1. MS (thermospray): M/Z [M+H] 372.1.
C16H10Cl2F3N2 +H zahtijeva 372,03. C16H10Cl2F3N2 +H requires 372.03.
Priprema 38 Preparation 38
5-amino-1-(2,6-dikloro-4-trifluorometilfenil)-4-jodo-3-fenilpirazol 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodo-3-phenylpyrazole
Dobiven je iz spoja iz naslova pripreme 37, analogno sa pripremom 1, osim Å”to je reakcijska smjesa mijeÅ”ana tokom 18 sati, kao žuti Ävrsti proizvod, t.t. 162-164 Ā°C. It was obtained from the title compound of preparation 37, analogously to preparation 1, except that the reaction mixture was stirred for 18 hours, as a yellow solid product, m.p. 162-164 Ā°C.
Ī“ (CDCl3): 3,80 (br.s, 2H); 7,35 (m, 3H); 7,78 (s, 2H); 7,95 (m, 2H). Ī“ (CDCl 3 ): 3.80 (no.s, 2H); 7.35 (m, 3H); 7.78 (s, 2H); 7.95 (m, 2H).
MS (termosprej): M/Z [M+H] 498,1. MS (thermospray): M/Z [M+H] 498.1.
C16H9Cl2F3IN3 +H zahtijeva 497,93. C16H9Cl2F3IN3 +H requires 497.93.
Priprema 39 Preparation 39
1-(2,6-dikloro-4-trifluorometilfenil)-4-jodo-3-fenilpirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-iodo-3-phenylpyrazole
Otopina t-butil nitrita (3,0 g) u tetrahidrofuranu (20 ml) dodana je ukapavanjem tokom 30 minuta u izmijeÅ”anu otopinu spoja iz naslova pripreme 38 (2,5 g) u tetrahidrofuranu (50 ml) na 65 Ā°C. Nakon daljnja 3 sata na 65 Ā°C, reakcijska smjesa je ostavljena da se hladi, držana je na sobnoj temperaturi tokom 18 sati i zatim isparena pod sniženim tlakom. RezultirajuÄe ulje je proÄiÅ”Äeno dvjema operacijama kromatografije stupca na silikagelu, prvo koristeÄi diklorometan kao eluant i zatim sekvencijalno, heksan, heksan:etil acetat (95:5) i heksan:etil acetat (90:10) kao eluante, radi dobivanja spoja iz naslova kao Ävrsta krema. t.t. 88-89 Ā°C. A solution of t-butyl nitrite (3.0 g) in tetrahydrofuran (20 ml) was added dropwise over 30 minutes to a stirred solution of the title compound 38 (2.5 g) in tetrahydrofuran (50 ml) at 65 Ā°C. After a further 3 hours at 65 Ā°C, the reaction mixture was allowed to cool, kept at room temperature for 18 hours and then evaporated under reduced pressure. The resulting oil was purified by two silica gel column chromatography operations, first using dichloromethane as eluent and then sequentially, hexane, hexane:ethyl acetate (95:5) and hexane:ethyl acetate (90:10) as eluants, to afford the title compound as solid cream. d.p. 88-89 Ā°C.
Ī“ (CDCl3): 7,45 (m, 3H); 7,70 (s, 1H); 7,72 (s, 2H); 7,95 (m, 2H). Ī“ (CDCl 3 ): 7.45 (m, 3H); 7.70 (s, 1H); 7.72 (s, 2H); 7.95 (m, 2H).
MS (termosprej): M/Z [M+H] 482,8. MS (thermospray): M/Z [M+H] 482.8.
C16H8Cl2F3IN2 +NH zahtijeva 482,91. C16H8Cl2F3IN2 +NH requires 482.91.
Priprema 40 Preparation 40
1-(2,6-dikloro-4-trifluorometilfenil)-4-etenil-3-fenilpirazol 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethenyl-3-phenylpyrazole
Tetrakis(trifenilfosfin)paladij(0) (0,07 g) dodan je u izmijeÅ”anu otopinu spoja iz naslova iz pripreme 39 (1,0 g) u dimetilformamidu (12 ml) na sobnoj temperaturi praÄeno, 10 minuta kasnije, sa tri-n-butil(vinil)kositrom (1,8 ml). RezultirajuÄa smjesa je grijana na 70 Ā°C tokom 6 sati, ostavljena je da stoji na sobnoj temperaturi tokom 18 sati, zatim je isparena pod sniženim tlakom. Ostatak je podijeljen izmeÄu diklorometana (50 ml) i vode (50 ml), zatim je organska faza izdvojena, osuÅ”ena (MgSO4) i isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen dvjema operacijama kromatografije stupca na silikagelu, prvo koristeÄi gradijent elucije etil acetata u heksanu i drugo koristeÄi gradijent elucije etera u heksanu, radi dobivanja spoja iz naslova kao žuto ulje. Tetrakis(triphenylphosphine)palladium(0) (0.07 g) was added to a stirred solution of the title compound from Preparation 39 (1.0 g) in dimethylformamide (12 mL) at room temperature followed, 10 minutes later, by tri-n -butyl(vinyl)tin (1.8 ml). The resulting mixture was heated at 70 Ā°C for 6 hours, left to stand at room temperature for 18 hours, then evaporated under reduced pressure. The residue was partitioned between dichloromethane (50 ml) and water (50 ml), then the organic phase was separated, dried (MgSO 4 ) and evaporated under reduced pressure. The residue was purified by two silica gel column chromatography operations, first using a gradient elution of ethyl acetate in hexane and second using a gradient elution of ether in hexane, to give the title compound as a yellow oil.
Ī“ (CDCl3): 5,25 (d, 1H); 5,65 (d, 1H); 6,80 (dd, 1H); 7,45 (m, 3H); 7,75 (m, 5H). Ī“ (CDCl 3 ): 5.25 (d, 1H); 5.65 (d, 1H); 6.80 (dd, 1H); 7.45 (m, 3H); 7.75 (m, 5H).
MS (termosprej): M/Z [M+H] 383,3. MS (thermospray): M/Z [M+H] 383.3.
C18H11Cl2F3N2 +H zahtijeva 383,03. C18H11Cl2F3N2 +H requires 383.03.
Priprema 41 Preparation 41
5-amino-4-klorodifluoroacetil-3-ciano-1-(2,6 dikloro-4-trifluorometilfenil)pirazol 5-amino-4-chlorodifluoroacetyl-3-cyano-1-(2,6 dichloro-4-trifluoromethylphenyl)pyrazole
Klorodifluorocteni anhidrid (30,37 g) je dodan ukapavanjem u izmijeÅ”anu, ledom-ohlaÄenu otopinu 5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazola (EP-A-0295117; 20,0 g) u piridinu (200 ml), zatim je reakcijska smjesa mijeÅ”ana na sobnoj temperaturi tokom 16 sati. RezultirajuÄa smjesa je koncentrirana uklanjanjem piridina (150 ml) pod sniženim tlakom, zatim je sipana u izmijeÅ”ani led/voda (500 ml). pH ove smjese je podeÅ”en na 1 dodatnim ukapavanjem koncentrirane klorovodiÄne kiseline (30 ml), sa mijeÅ”anjem, i izvrÅ”enom ekstrakcijom sa etil acetatom (2 Ć 500 ml). Kombinirani organski ekstrakti su isprani sa zasiÄenom vodenom otopinom natrij bikarbonata (500 ml), osuÅ”eni (MgSO4) i ispareni pod sniženim tlakom. Ostatak je otopljen u smjesi tetrahidrofurana (200 ml) i vode (50 ml), zatim je otopina zagrijavana na 60 Ā°C tokom 16 sati, ostavljena da se hladi i veÄi dio tetrahidrofurana je uklonjeno isparavanjem pod sniženim tlakom. Ekstrakcija sa etil acetatom (2 Ć 300 ml) je izvrÅ”ena, zatim su kombinirani organski ekstrakti isprani sekvencijalno sa vodom (100 ml) i slanom vodom (2 Ć 100 ml), osuÅ”eni (MgSO4) i ispareni pod sniženim tlakom. RezultirajuÄi ostatak je kristaliziran iz propan-2-ola radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 225-226 Ā°C. Chlorodifluoroacetic anhydride (30.37 g) was added dropwise to a stirred, ice-cooled solution of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole (EP-A-0295117; 20.0 g) in pyridine (200 ml), then the reaction mixture was stirred at room temperature for 16 hours. The resulting mixture was concentrated by removing pyridine (150 ml) under reduced pressure, then poured into mixed ice/water (500 ml). The pH of this mixture was adjusted to 1 by additional drops of concentrated hydrochloric acid (30 ml), with stirring, and extraction with ethyl acetate (2 x 500 ml). The combined organic extracts were washed with saturated aqueous sodium bicarbonate solution (500 ml), dried (MgSO4) and evaporated under reduced pressure. The residue was dissolved in a mixture of tetrahydrofuran (200 ml) and water (50 ml), then the solution was heated to 60 Ā°C for 16 hours, allowed to cool and most of the tetrahydrofuran was removed by evaporation under reduced pressure. Extraction with ethyl acetate (2 x 300 ml) was performed, then the combined organic extracts were washed sequentially with water (100 ml) and brine (2 x 100 ml), dried (MgSO4) and evaporated under reduced pressure. The resulting residue was crystallized from propan-2-ol to give the title compound as a white solid, m.p. 225-226 Ā°C.
Ī“ (CDCl3): 6,08 (br.s, 2H); 7,84 (s, 2H). Ī“ (CDCl 3 ): 6.08 (no.s, 2H); 7.84 (s, 2H).
MS (termosprej): M/Z [M+NH4] 450,1. MS (thermospray): M/Z [M+NH4] 450.1.
C13H4Cl3F5N4O+NH4 zahtijeva 450,0. C13H4Cl3F5N4O+NH4 requires 450.0.
Priprema 42 Preparation 42
4-klorodifluoroacetil-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 4-chlorodifluoroacetyl-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
t-butil nitrit (12,45 ml) je dodan ukapavanjem u izmijeÅ”anu otopinu spoja iz naslova pripreme 41 (13,7 g) u tetrahidrofuranu (100 ml) i smjesa je grijana na 60 Ā°C tokom 22 sata, ostavljena da se ohladi i isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (50 g), koristeÄi diklorometan kao eluant, praÄeno trituracijom sa heksanom (5 Ć 50 ml) i kristalizacijom iz diklorometana, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 124-125 Ā°C. t-Butyl nitrite (12.45 ml) was added dropwise to a stirred solution of the title compound of Preparation 41 (13.7 g) in tetrahydrofuran (100 ml) and the mixture was heated at 60 Ā°C for 22 hours, allowed to cool and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (50 g) using dichloromethane as eluent, followed by trituration with hexane (5 x 50 ml) and crystallization from dichloromethane to give the title compound as a white solid, m.p. 124-125 Ā°C.
Ī“ (CDCl3): 7,83 (s, 2H); 8,27 (s, 1H). Ī“ (CDCl 3 ): 7.83 (s, 2H); 8.27 (s, 1H).
MS (termosprej): M/Z [M+NH4] 435,2. MS (thermospray): M/Z [M+NH 4 ] 435.2.
C13H3Cl3F5N5O+NH4 zahtijeva 435,0. C13H3Cl3F5N5O+NH4 requires 435.0.
Priprema 43 Preparation 43
4-(3-kloro-3,3-difluoropropen-2-il)-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 4-(3-chloro-3,3-difluoropropen-2-yl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
2,5 M otopine n-butilitija u heksanu (3,8 ml) dodano je ukapavanjem u izmijeÅ”anu suspenziju metiltrifenilfosfonij jodida (3,817 g) u tetrahidrofuranu (20 ml) pod duÅ”ikom na sobnoj temperaturi. RezultirajuÄa crvenkasto smeÄa otopina dodana je ukapavanjem, pod duÅ”ikom, u izmijeÅ”anu otopinu spoja iz naslova pripreme 42 (3,95 g) u tetrahidrofuranu (30 ml) na sobnoj temperaturi i reakcijska smjesa je mijeÅ”ana tokom 1 sata. Voda (50 ml) je zatim dodana, ekstrakcija sa eterom (2 Ć 50 ml) je izvrÅ”ena i kombinirani organski ekstrakti su osuÅ”eni (Na2SO4) i ispareni pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (100 g), koristeÄi heksan:diklorometan (1:1) kao eluant, praÄeno kristalizacijom iz propan-2-ola, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 113-114 Ā°C. A 2.5 M solution of n-butyllithium in hexane (3.8 ml) was added dropwise to a stirred suspension of methyltriphenylphosphonium iodide (3.817 g) in tetrahydrofuran (20 ml) under nitrogen at room temperature. The resulting reddish brown solution was added dropwise, under nitrogen, to a stirred solution of the title compound 42 (3.95 g) in tetrahydrofuran (30 mL) at room temperature and the reaction mixture was stirred for 1 hour. Water (50 ml) was then added, extraction with ether (2 x 50 ml) was carried out and the combined organic extracts were dried (Na 2 SO 4 ) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (100 g), using hexane:dichloromethane (1:1) as eluent, followed by crystallization from propan-2-ol, to afford the title compound as a white solid, m.p. 113-114 Ā°C.
Ī“ (CDCl3): 6,12 (s, 1H); 6,20 (s, 1H); 7,75 (s, 2H); 7,80 (s, 1H). Ī“ (CDCl 3 ): 6.12 (s, 1H); 6.20 (s, 1H); 7.75 (s, 2H); 7.80 (s, 1H).
MS (termosprej): M/Z [M+NH4] 433,0. MS (thermospray): M/Z [M+NH 4 ] 433.0.
C14H5Cl3F5N3 + NH4 zahtijeva 433,0. C14H5Cl3F5N3 + NH4 requires 433.0.
Priprema 44 Preparation 44
4-(3-klorodifluorometil-1-pirazolin-3-il)-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 4-(3-chlorodifluoromethyl-1-pyrazolin-3-yl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Otopina diazometana u eteru (7,0 ml, 2,3 mmol) dodana je polako u izmijeÅ”anu otopinu spoja iz naslova pripreme 43 (800 mg) u eteru (10 ml) na sobnoj temperaturi i smjesa je mijeÅ”ana tokom 1 sata. ViÅ”kovi diazometana i otapala su ispareni pod stalnim strujanjem duÅ”ika radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod. A solution of diazomethane in ether (7.0 mL, 2.3 mmol) was added slowly to a stirred solution of the title compound 43 (800 mg) in ether (10 mL) at room temperature and the mixture was stirred for 1 hour. Excess diazomethane and solvent were evaporated under a constant stream of nitrogen to afford the title compound as a white solid.
Ī“ (CDCl3): 2,27 (m, 1H); 2,58 (m, 1H); 4,90 (m, 2H); 7,75 (s, 2H); 8,06 (s, 1H). Ī“ (CDCl 3 ): 2.27 (m, 1H); 2.58 (m, 1H); 4.90 (m, 2H); 7.75 (s, 2H); 8.06 (s, 1H).
MS (termosprej): M/Z [M+NH4] 474,8. MS (thermospray): M/Z [M+NH 4 ] 474.8.
C15H7Cl3F5N5 +NH4 zahtijeva 475,0. C15H7Cl3F5N5 +NH4 requires 475.0.
Priprema 45 Preparation 45
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-propanoilpirazol 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-propanoylpyrazole
Monohidrat p-toluensulfonske kiseline (2,92 g) je dodan u izmijeÅ”anu otopinu 5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(prop-1-in-l-il)pirazola (WO-A-97/07102; 2,1 g) u acetonitrilu (40 ml) i smjesa je mijeÅ”ana na sobnoj temperaturi tokom 1 sata. Daljnji monohidrat p-toluensulfonske kiseline (1,0 ) je dodan i smjesa je mijeÅ”ana na sobnoj temperaturi tokom 16 sati. Daljnji acetonitril (20 ml) i joÅ” monohidrat p-toluensulfonske kiseline (1,0 g) su dodani i mijeÅ”anje je nastavljeno tokom 1 sata, zatim je reakcijska smjesa sipana u zasiÄenu vodenu otopinu natrij bikarbonata (500 ml) i ekstrahirana je sa eterom (2 Ć 100 ml). Kombinirani organski ekstrakti su isprani sa slanom vodom (100 ml), osuÅ”eni (Na2SO4) i ispareni pod sniženim tlakom, zatim je ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu (70 g), koristeÄi diklorometan kao eluant, radi dobivanja spoja iz naslova kao blijedo smeÄi Ävrsti proizvod, t.t. 167-169 Ā°C. p-toluenesulfonic acid monohydrate (2.92 g) was added to the stirred solution of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(prop-1-yn-1-yl )pyrazole (WO-A-97/07102; 2.1 g) in acetonitrile (40 ml) and the mixture was stirred at room temperature for 1 hour. Further p-toluenesulfonic acid monohydrate (1.0) was added and the mixture was stirred at room temperature for 16 hours. Further acetonitrile (20 ml) and more p-toluenesulfonic acid monohydrate (1.0 g) were added and stirring was continued for 1 hour, then the reaction mixture was poured into saturated aqueous sodium bicarbonate (500 ml) and extracted with ether ( 2 x 100 ml). The combined organic extracts were washed with brine (100 ml), dried (Na2SO4) and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel (70 g) using dichloromethane as eluent to give the title compound as a pale brown solid product, m.p. 167-169 Ā°C.
Ī“ (CDCl3): 1,26 (t, 3H); 3,03 (q, 2H); 5,83 (br.s, 2H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 1.26 (t, 3H); 3.03 (q, 2H); 5.83 (no.s, 2H); 7.80 (s, 2H).
MS (termosprej): M/Z [M+H] 377,2. MS (thermospray): M/Z [M+H] 377.2.
C14H9Cl2F3N4O + H zahtijeva 377,0. C14H9Cl2F3N4O + H requires 377.0.
Priprema 46 Preparation 46
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-propanoilpirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-propanoylpyrazole
T-butil nitrit (0,66 ml) dodan je ukapavanjem u izmijeÅ”anu otopinu spoja iz naslova pripreme 45 (1,2 g) u tetrahidrofuranu (30 ml) i smjesa je mijeÅ”ana na sobnoj temperaturi tokom 1 sata. Daljnji t-butil nitrit (0,3 ml) je dodan i smjesa je mijeÅ”ana na sobnoj temperaturi tokom 1 sata. Dalje, reakcijska smjesa je grijana na 60 Ā°C tokom 10 minuta, ostavljena da se ohladi i isparena je pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu (50 g), koristeÄi diklorometan kao eluant, radi dobivanja spoja iz naslova kao vrlo blijedi žuti Ävrst proizvod, t.t. 143 Ā°C. T-butyl nitrite (0.66 ml) was added dropwise to a stirred solution of the title compound 45 (1.2 g) in tetrahydrofuran (30 ml) and the mixture was stirred at room temperature for 1 hour. Further t-butyl nitrite (0.3 ml) was added and the mixture was stirred at room temperature for 1 hour. Next, the reaction mixture was heated to 60 Ā°C for 10 minutes, allowed to cool and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (50 g), using dichloromethane as eluent, to afford the title compound as a very pale yellow solid, m.p. 143 Ā°C.
Ī“ (CDCl3): 1,28 (m, 3H); 3,01 (q, 2H); 7,80 (s, 2H); 8,15 (s, 1H). Ī“ (CDCl 3 ): 1.28 (m, 3H); 3.01 (q, 2H); 7.80 (s, 2H); 8.15 (s, 1H).
MS (termosprej): M/Z [M+NH4] 379,3. MS (thermospray): M/Z [M+NH 4 ] 379.3.
C14H8Cl2F3N3O + NH4 zahtijeva 379,0. C14H8Cl2F3N3O + NH4 requires 379.0.
Priprema 47 Preparation 47
4-(but-l-en-2-il)-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)pirazol 4-(but-1-en-2-yl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole
Dobiven je iz spoja iz naslova pripreme 46, analogno sa pripremom 43 ali koristeÄi heksan:diklorometan (2:3) kao kromatografski eluant i bez dalje kristalizacije, kao bijeli Ävrsti proizvod, t.t. 104-105 Ā°C. It was obtained from the title compound of preparation 46, analogously to preparation 43 but using hexane:dichloromethane (2:3) as chromatographic eluent and without further crystallization, as a white solid product, m.p. 104-105 Ā°C.
Ī“ (CDCl3): 1,19 (t, 3H); 2,47 (q, 2H); 5,29 (s, 1H); 5,74 (s, 1H); 7,60 (s, 1H); 7,79 (s, 2H). Ī“ (CDCl 3 ): 1.19 (t, 3H); 2.47 (q, 2H); 5.29 (s, 1H); 5.74 (s, 1H); 7.60 (s, 1H); 7.79 (s, 2H).
MS (termosprej): M/Z [M+H] 360,1. MS (thermospray): M/Z [M+H] 360.1.
C15H10Cl2F3N3 +H zahtijeva 360,0. C15H10Cl2F3N3 +H requires 360.0.
Priprema 48 Preparation 48
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-pentafluoropropanoilpirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-pentafluoropropanoylpyrazole
2,5 M otopina n-butilitija u heksanu (2,78 ml) dodana je u izmijeÅ”anu otopinu spoja iz naslova pripreme 3 (3,0 g) u tetrahidrofuranu (80 ml) na -80 Ā°C, pod duÅ”ikom, takvom brzinom da temperatura reakcijske smjese nije preÅ”la -73 Ā°C. Smjesa je mijeÅ”ana na -73 Ā°C tokom 10 minuta i zatim je dodana otopina metil pentafluoropropionata (0,89 ml) u tetrahidrofuranu (5 ml) takvom brzinom da temperatura reakcijske smjese nije preÅ”la -75 Ā°C. Nakon zavrÅ”etka dodavanja, smjesa je ostavljena da se zagrije na sobnu temperaturu tokom perioda od 1,5 sata, zatim je dodana voda (100 ml) i rezultirajuÄa smjesa je ekstrahirana sa etil acetatom (2 Ć 80 ml). Kombinirani organski slojevi su osuÅ”eni (Na2SO4) i ispareni pod sniženim tlakom, zatim je ostatak proÄiÅ”Äen kromatografijom stupca na silikagelu (150 g), koristeÄi heksan:diklorometan (1:9) kao eluant, i dalje je proÄiÅ”Äen kromatografijom stupca na silikagelu (50 g), koristeÄi heksan:eter (9:1) kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 120 Ā°C. A 2.5 M solution of n-butyllithium in hexane (2.78 ml) was added to a stirred solution of the title compound 3 (3.0 g) in tetrahydrofuran (80 ml) at -80 Ā°C, under nitrogen, at such a rate that the temperature of the reaction mixture did not exceed -73 Ā°C. The mixture was stirred at -73 Ā°C for 10 minutes and then a solution of methyl pentafluoropropionate (0.89 ml) in tetrahydrofuran (5 ml) was added at such a rate that the temperature of the reaction mixture did not exceed -75 Ā°C. After the addition was complete, the mixture was allowed to warm to room temperature over a period of 1.5 hours, then water (100 ml) was added and the resulting mixture was extracted with ethyl acetate (2 x 80 ml). The combined organic layers were dried (Na2SO4) and evaporated under reduced pressure, then the residue was purified by column chromatography on silica gel (150 g), using hexane:dichloromethane (1:9) as eluant, and further purified by column chromatography on silica gel (50 g ), using hexane:ether (9:1) as eluent, to afford the title compound as a white solid, m.p. 120 Ā°C.
Ī“ (CDCl3): 7,80 (s, 2H); 8,25 (s, 1H). Ī“ (CDCl 3 ): 7.80 (s, 2H); 8.25 (s, 1H).
MS (termosprej): M/Z [M+NH4] 468,9. MS (thermospray): M/Z [M+NH 4 ] 468.9.
C14H3Cl2F8N3O + NH4 zahtijeva 469,0. C14H3Cl2F8N3O + NH4 requires 469.0.
Priprema 49 Preparation 49
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(3,3,4,4,4-pentafluorobut-1-en-2-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3,3,4,4,4-pentafluorobut-1-en-2-yl)pyrazole
Dobiven je od spoja iz naslova pripreme 48, analogno sa pripremom 43 ali bez bilo kakve poslije-kromatografske kristalizacije, kao bijeli Ävrsti proizvod, t.t. 107-108 Ā°C. It was obtained from the title compound of preparation 48, analogously to preparation 43 but without any post-chromatographic crystallization, as a white solid, m.p. 107-108 Ā°C.
Ī“ (CDCl3): 6,23 (s, 1H); 6,43 (s, 1H); 7,73 (s, 1H); 7,79 (s, 2H). Ī“ (CDCl 3 ): 6.23 (s, 1H); 6.43 (s, 1H); 7.73 (s, 1H); 7.79 (s, 2H).
MS (elektrosprej): M/Z [M+H] 450,0. MS (electrospray): M/Z [M+H] 450.0.
C15H5Cl2F8N3 + H zahtijeva 450,0. C15H5Cl2F8N3 + H requires 450.0.
Priprema 50 Preparation 50
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(3-pentafluoroetil-1-pirazolin-3-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3-pentafluoroethyl-1-pyrazolin-3-yl)pyrazole
Dobiven je od spoja iz naslova pripreme 49, analogno sa pripremom 44, kao bijeli Ävrsti proizvod. It was obtained from the title compound of preparation 49, analogously to preparation 44, as a white solid product.
Ī“ (CDCl3): 2,26 (m, 1H); 2,61 (m, 1H); 4,83 (m, 2H); 7,76 (s, 2H); 7,98 (s, 1H). Ī“ (CDCl 3 ): 2.26 (m, 1H); 2.61 (m, 1H); 4.83 (m, 2H); 7.76 (s, 2H); 7.98 (s, 1H).
MS (termosprej): M/Z [M+H] 491,8. MS (thermospray): M/Z [M+H] 491.8.
C16H7Cl2F8N5 + H zahtijeva 492,0. C16H7Cl2F8N5 + H requires 492.0.
Priprema 51 Preparation 51
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-heptafluorobutanoilpirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-heptafluorobutanoylpyrazole
Dobiven je od spoja iz naslova pripreme 3 i metil heptafluorobutirata, analogno sa pripremom 48 ali koristeÄi heksan:eter (2:3) kao eluanta u prvoj fazi kromatografskog proÄiÅ”Äavanja i gradijentom elucije heksan:etera (19:1 do 9:1) u drugoj takvoj fazi, kao blijedo žuti Ävrsti proizvod, t.t. 102-103 Ā°C. It was obtained from the compound from the title of preparation 3 and methyl heptafluorobutyrate, analogous to preparation 48 but using hexane:ether (2:3) as eluent in the first stage of chromatographic purification and gradient elution of hexane:ether (19:1 to 9:1) in the second. such phase, as a pale yellow solid product, m.p. 102-103 Ā°C.
Ī“ (CDCl3): 7,80 (s, 2H); 8,24 (s, 1H). Ī“ (CDCl 3 ): 7.80 (s, 2H); 8.24 (s, 1H).
MS (termosprej): M/Z [M+NH4] 518,7. MS (thermospray): M/Z [M+NH 4 ] 518.7.
C15H3Cl2F10N3O + NH4 zahtijeva 519,0. C15H3Cl2F10N3O + NH4 requires 519.0.
Priprema 52 Preparation 52
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(3,3,4,4,5,5,5-heptafluoropent-1-en-2-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3,3,4,4,5,5,5-heptafluoropent-1-en-2-yl)pyrazole
Dobiven je od spoja iz naslova pripreme 51, analogno sa pripremom 43, ali koristeÄi diklorometan kao eluant u prvoj fazi kromatografskog proÄiÅ”Äavanja i heksan:diklorometan (1:1) kao eluant u drugoj takvoj fazi, bez dalje kristalizacije, kao bijeli Ävrsti proizvod, t.t. 109-110Ā°C. It was obtained from the title compound of preparation 51, analogously to preparation 43, but using dichloromethane as eluent in the first stage of chromatographic purification and hexane:dichloromethane (1:1) as eluent in the second such stage, without further crystallization, as a white solid product, m.p. 109-110Ā°C.
Ī“ (CDCl3): 6,24 (s, 1H); 6,43 (s, 1H); 7,73 (s, 1H); 7,80 (s, 2H). Ī“ (CDCl 3 ): 6.24 (s, 1H); 6.43 (s, 1H); 7.73 (s, 1H); 7.80 (s, 2H).
MS (elektrosprej): M/Z [M+H] 500,0. MS (electrospray): M/Z [M+H] 500.0.
C16H5Cl2F10N3 + NH zahtijeva 500. C16H5Cl2F10N3 + NH requires 500.
Priprema 53 Preparation 53
3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(3-heptafluoropropil-1-pirazolin-3-il)pirazol 3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3-heptafluoropropyl-1-pyrazolin-3-yl)pyrazole
Dobiven je od spoja iz naslova pripreme 52, analogno sa pripremom 44, kao bijeli Ävrsti proizvod. It was obtained from the title compound of preparation 52, analogously to preparation 44, as a white solid product.
Ī“ (CDCl3): 2,36 (m, 1H); 2,58 (m, 1H); 4,80 (m, 1H); 4,87 (m, 1H); 7,77 (s, 2H); 7,98 (s, 1H). Ī“ (CDCl 3 ): 2.36 (m, 1H); 2.58 (m, 1H); 4.80 (m, 1H); 4.87 (m, 1H); 7.77 (s, 2H); 7.98 (s, 1H).
MS (termosprej): M/Z [M+NH4] 559,3. MS (thermospray): M/Z [M+NH4] 559.3.
C17H7Cl2F10N5 + NH4 zahtijeva 559,0. C17H7Cl2F10N5 + NH4 requires 559.0.
Priprema 54 Preparation 54
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(3,3,3,-trifluoropropen-2-il)pirazol 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3,3,3,-trifluoropropen-2-yl)pyrazole
Otopina 3,3,3-trifluoropropen-2-il cink bromida: N,N,N',N'-tetrametiletilenediamin kompleks u tetrahidrofuranu ("J. Org. Chem.", 56, 7336, (1991.); 4,5 ml, 5 mmol) dodana je u izmijeÅ”anu otopinu spoja iz naslova pripreme 1 (1,0 g) i tetrakis(trifenilfosfin)paladija(0) (60 mg) u nevodenom tetrahidrofuranu (1,0 ml), pod duÅ”ikom, i reakcijska smjesa je grijana na 55 Ā°C tokom 20 sati, ostavljena da se ohladi i sipana u izmijeÅ”ani heksan (50 ml). RezultirajuÄa smjesa je filtrirana, filterski umetak je ispran sa eterom (50 ml) i kombinirane organske otopine su isparene pod sniženim tlakom. Ostatak je proÄiÅ”Äen dvijema kromatografskim operacijama stupca na silikagelu (40 g, zatim 10 g), prvo koristeÄi heksan:eter:diklorometan (4:1:1) kao eluanta zatim, sekvencijalno, heksan, heksan:eter (4:1) i heksan:eter:diklorometan (4:1:1) kao eluante, radi dobivanja spoja iz naslova kao vrlo blijedo žuti Ävrsti proizvod, t.t. 147-148 Ā°C. A solution of 3,3,3-trifluoropropen-2-yl zinc bromide: N,N,N',N'-tetramethylethylenediamine complex in tetrahydrofuran ("J. Org. Chem.", 56, 7336, (1991); 4, 5 ml, 5 mmol) was added to a mixed solution of the compound from the title of preparation 1 (1.0 g) and tetrakis(triphenylphosphine)palladium(0) (60 mg) in anhydrous tetrahydrofuran (1.0 ml), under nitrogen, and the reaction the mixture was heated at 55 Ā°C for 20 hours, allowed to cool and poured into mixed hexane (50 ml). The resulting mixture was filtered, the filter insert was washed with ether (50 mL) and the combined organic solutions were evaporated under reduced pressure. The residue was purified by two column chromatography operations on silica gel (40 g, then 10 g), first using hexane:ether:dichloromethane (4:1:1) as eluent, then, sequentially, hexane, hexane:ether (4:1) and hexane :ether:dichloromethane (4:1:1) as eluent, to give the title compound as a very pale yellow solid, m.p. 147-148 Ā°C.
Ī“ (CDCl3): 3,93 (br.s, 2H); 5,96 (s, 1H); 6,24 (s, 1H); 7,78 (s, 2H). Ī“ (CDCl 3 ): 3.93 (no.s, 2H); 5.96 (s, 1H); 6.24 (s, 1H); 7.78 (s, 2H).
MS (termosprej): M/Z [M+H] 415,0. MS (thermospray): M/Z [M+H] 415.0.
C14H6Cl2F6N4 + H zahtijeva 415,0. C14H6Cl2F6N4 + H requires 415.0.
Priprema 55 Preparation 55
5-amino-3-ciano-1-(2,6-dikloro-4-trifluorometilfenil)-4-(3-trifluorometil-1-pirazolin-3-il)pirazol 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3-trifluoromethyl-1-pyrazolin-3-yl)pyrazole
Dobiven je od spoja iz naslova pripreme 54, analogno sa pripremom 44, kao bijeli Ävrsti proizvod. It was obtained from the title compound of preparation 54, analogously to preparation 44, as a white solid product.
Ī“ (CDCl3): 2,28 (m, 1H); 2,60 (m, 1H); 4,77 (br.s, 2H); 4,77 (m, 1H); 5,02 (m, 1H); 7,78 (s, 1H); 7,82 (s, 1H). Ī“ (CDCl 3 ): 2.28 (m, 1H); 2.60 (m, 1H); 4.77 (no.s, 2H); 4.77 (m, 1H); 5.02 (m, 1H); 7.78 (s, 1H); 7.82 (s, 1H).
MS (termosprej): M/Z [M+H] 457,0. MS (thermospray): M/Z [M+H] 457.0.
C15H8Cl2F6N6 + H zahtijeva 457,0. C15H8Cl2F6N6 + H requires 457.0.
Priprema 56 Preparation 56
5-amino-1-[(3-kloro-5-trifluorometil)piridin-2-il]-3-ciano-4-jodopirazol 5-amino-1-[(3-chloro-5-trifluoromethyl)pyridin-2-yl]-3-cyano-4-iodopyrazole
N-jodosukcinimid (10 g) dodan je u izmijeÅ”anu otopinu 5-amino-1-[(3-kloro-5-trifluorometil)piridin-2-il]-3-cianopirazola (EP-A-0500209; 7,91 g) u acetonitrilu (100 ml) na sobnoj temperaturi. Nakon 16 sati, reakcijska smjesa je isparena pod sniženim tlakom, preostali Ävrsti materijal je otopljen u diklorometanu i rezultirajuÄa otopina je isprana sukcesivno sa vodenom otopinom natrij tiosulfata (Ć 2), vodom i zasiÄenom slanom vodom, osuÅ”ena (MgSO4) i isparena pod sniženim tlakom radi dobivanja spoja iz naslova kao ružiÄasti Ävrsti proizvod, t.t. 107-108 Ā°C. N-iodosuccinimide (10 g) was added to a stirred solution of 5-amino-1-[(3-chloro-5-trifluoromethyl)pyridin-2-yl]-3-cyanopyrazole (EP-A-0500209; 7.91 g) in acetonitrile (100 ml) at room temperature. After 16 hours, the reaction mixture was evaporated under reduced pressure, the remaining solid material was dissolved in dichloromethane and the resulting solution was washed successively with aqueous sodium thiosulfate (Ć 2), water and saturated brine, dried (MgSO4) and evaporated under reduced pressure to afford the title compound as a pink solid, m.p. 107-108 Ā°C.
Ī“ (CDCl3) 5,15 (br.s, 2H); 8,20 (s, 1H); 8,67 (s, 1H). Ī“ (CDCl 3 ) 5.15 (no.s, 2H); 8.20 (s, 1H); 8.67 (s, 1H).
MS (termosprej): M/Z [M+H] 413,1. MS (thermospray): M/Z [M+H] 413.1.
C10H4CIF3IN5 +H zahtijeva 412,9. C10H4CIF3IN5 +H requires 412.9.
Priprema 57 Preparation 57
1-[(3-kloro-5-trifluorometil)piridin-2-il]-3-ciano-4-jodopirazol 1-[(3-chloro-5-trifluoromethyl)pyridin-2-yl]-3-cyano-4-iodopyrazole
Otopina t-butil nitrita (7,2 ml) u tetrahidrofuranu (30 ml) dodana je ukapavanjem u izmijeÅ”anu smjesu spoja iz naslova pripreme 56 (12,5 g) u tetrahidrofuranu (90 ml) koji je blago zagrijan do refluksa, zatim je reakcijska smjesa ostavljena da se ohladi na sobnu temperaturu i isparena je pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:etil acetat (4:1) kao eluant, radi dobivanja spoja iz naslova kao žuti Ävrsti proizvod, t.t. 104-107 Ā°C. A solution of t-butyl nitrite (7.2 ml) in tetrahydrofuran (30 ml) was added dropwise to a stirred mixture of the compound from the title of preparation 56 (12.5 g) in tetrahydrofuran (90 ml) which was slightly heated to reflux, then the reaction the mixture was allowed to cool to room temperature and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, using hexane:ethyl acetate (4:1) as eluant, to give the title compound as a yellow solid, m.p. 104-107 Ā°C.
Ī“ (CDCl3): 8,20 (s, 1H); 8,70 (s, 1H). Ī“ (CDCl 3 ): 8.20 (s, 1H); 8.70 (s, 1H).
MS (termosprej): M/Z [M+H] 397,8. MS (thermospray): M/Z [M+H] 397.8.
C10H3CIF3IN4 +H zahtijeva 397,9. C10H3CIF3IN4 +H requires 397.9.
Priprema 58 Preparation 58
1-[(3-kloro-5-trifluorometil)piridin-2-il]-3-ciano-4-etenilpirazol 1-[(3-chloro-5-trifluoromethyl)pyridin-2-yl]-3-cyano-4-ethenylpyrazole
Tri-n-butil(vinil)kositar (9,19 g) i tetrakis(trifenilfosfin)paladij0) (0,3 g) dodani su u izmijeÅ”anu otopinu spoja iz naslova pripreme 57 (10,50 g) u dimetilformamidu (100 ml) na sobnoj temperaturi, pod duÅ”ikom, i rezultirajuÄa smjesa je grijana na 75 Ā°C tokom 16 sati, zatim je ostavljena da se ohladi. Smjesa je isparena pod sniženim tlakom, ostatak je podijeljen izmeÄu diklorometana i vode, zatim je izdvojena organska faza isprana sukcesivno sa vodom (Ć 3) i zasiÄenom slanom vodom, osuÅ”ena (MgSO4) i isparena pod sniženim tlakom. Ostatak je proÄiÅ”Äen kromatografijom stupca na silikagelu, koristeÄi heksan:etil acetat (9:1) kao eluant, radi dobivanja spoja iz naslova kao bijeli Ävrsti proizvod, t.t. 57,5-58,5 Ā°C. Tri-n-butyl(vinyl)tin (9.19 g) and tetrakis(triphenylphosphine)palladium (0.3 g) were added to a stirred solution of the title compound of Preparation 57 (10.50 g) in dimethylformamide (100 ml). at room temperature, under nitrogen, and the resulting mixture was heated at 75 Ā°C for 16 h, then allowed to cool. The mixture was evaporated under reduced pressure, the residue was partitioned between dichloromethane and water, then the separated organic phase was washed successively with water (Ć 3) and saturated brine, dried (MgSO4) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using hexane:ethyl acetate (9:1) as eluent to give the title compound as a white solid, m.p. 57.5-58.5 Ā°C.
Ī“ (CDCl3): 5,50 (d, 1H); 5,97 (d, 1H); 6,65 (dd, 1H); 8,20 (s, 1H); 8,35 (s, 1H); 8,70 (s, 1H). Ī“ (CDCl 3 ): 5.50 (d, 1H); 5.97 (d, 1H); 6.65 (dd, 1H); 8.20 (s, 1H); 8.35 (s, 1H); 8.70 (s, 1H).
MS (termosprej): M/Z [M+H] 297,9. MS (thermospray): M/Z [M+H] 297.9.
C12H6CIF3N4 + H zahtijeva 298,0. C12H6CIF3N4 + H requires 298.0.
Priprema 59 Preparation 59
5-amino-3-ciano-4-jodo-1-(2,4,6-triklorofenil)pirazol 5-amino-3-cyano-4-iodo-1-(2,4,6-trichlorophenyl)pyrazole
N-jodosukcinimid (17,67 g) dodan je u dijelovima u izmijeÅ”anu otopinu 5-amino-3-ciano-1-(2,4,6-triklorofenil)pirazola (US 5.232.940; 22,5 g) u acetonitrilu (300 ml) i rezultirajuÄa smjesa je mijeÅ”ana na sobnoj temperaturi tokom 1 sata, zatim je isparena pod sniženim tlakom. Ostatak je djelomiÄno proÄiÅ”Äen kromatografijom na silikagelu (800 g), koristeÄi gradijent elucije diklorometan:etil acetata (100:0 do 0:100), radi dobivanja blijedo smeÄeg Ävrstog proizvoda koji je dalje proÄiÅ”Äen kako slijedi. Trituracija sa heksanom (25 ml) dala je ostatak koji je otopljen u diklorometanu (500 ml). Ova otopina je isprana sa vodom (500 ml), vodeno ispiranje je ponovo isprano sa etil acetatom (500 ml) i kombinirane organske otopine su osuÅ”ene (Na2SO4) i isparene pod sniženim tlakom radi dobivanja spoja iz naslova kao blijedo smeÄi Ävrsti proizvod. N-iodosuccinimide (17.67 g) was added portionwise to a stirred solution of 5-amino-3-cyano-1-(2,4,6-trichlorophenyl)pyrazole (US 5,232,940; 22.5 g) in acetonitrile ( 300 ml) and the resulting mixture was stirred at room temperature for 1 hour, then evaporated under reduced pressure. The residue was partially purified by chromatography on silica gel (800 g), using a gradient elution of dichloromethane:ethyl acetate (100:0 to 0:100), to give a pale brown solid which was further purified as follows. Trituration with hexane (25 ml) gave a residue which was dissolved in dichloromethane (500 ml). This solution was washed with water (500 ml), the aqueous wash was washed again with ethyl acetate (500 ml) and the combined organic solutions were dried (Na 2 SO 4 ) and evaporated under reduced pressure to give the title compound as a pale brown solid.
Ī“ (DMSOd6): 6,28 (br.s, 2H); 7,98 (s, 2H). Ī“ (DMSOd 6 ): 6.28 (No.s, 2H); 7.98 (s, 2H).
MS (termosprej): M/Z [M+H] 413,0. MS (thermospray): M/Z [M+H] 413.0.
C10H4Cl3IN4 + H zahtijeva 412,9. C10H4Cl3IN4 + H requires 412.9.
Priprema 60 Preparation 60
3-ciano-4-jodo-1-(2,4,6-triklorofenil)pirazol 3-cyano-4-iodo-1-(2,4,6-trichlorophenyl)pyrazole
T-butil nitrit (7,13 ml) dodan je ukapavanjem tokom 5 minuta u izmijeÅ”anu otopinu spoja iz naslova pripreme 59 (15,5 g) u tetrahidrofuranu (400 ml), zatim je reakcijska smjesa mijeÅ”ana na sobnoj temperaturi tokom 1 sata, zagrijana na 60 Ā°C tokom 40 minuta, ostavljena da se ohladi i isparena je pod sniženim tlakom. RezultirajuÄi blijedo crveni Ävrsti proizvod je proÄiÅ”Äen kromatografijom stupca na silikagelu (500 g), koristeÄi diklorometan kao eluant, radi dobivanja spoja iz naslova kao blijedo žuti Ävrsti proizvod. T-butyl nitrite (7.13 ml) was added dropwise over 5 minutes to a mixed solution of the compound from the title of preparation 59 (15.5 g) in tetrahydrofuran (400 ml), then the reaction mixture was stirred at room temperature for 1 hour, heated at 60 Ā°C for 40 minutes, allowed to cool and evaporated under reduced pressure. The resulting pale red solid was purified by column chromatography on silica gel (500 g), using dichloromethane as eluent, to give the title compound as a pale yellow solid.
Ī“ (CDCl3): 7,52 (s, 2H); 7,67 (s, 1H). Ī“ (CDCl 3 ): 7.52 (s, 2H); 7.67 (s, 1H).
MS (termosprej): M/Z [M+NH4] 414,8. MS (thermospray): M/Z [M+NH 4 ] 414.8.
C10H3Cl3IN3 +NH4 zahtijeva 414,9. C10H3Cl3IN3 +NH4 requires 414.9.
Priprema 61 Preparation 61
3-ciano-4-etenil-1-(2,4,6-triklorofenil)pirazol 3-cyano-4-ethenyl-1-(2,4,6-trichlorophenyl)pyrazole
Smjesa spoja iz naslova pripreme 60 (10,8 g), tri-n-butil(vinil)kositra (20 ml), tetrakis(trifenilfosfin)paladija(0) (1,0 g) i dimetilformamida (60 ml) mijeÅ”ana je na 75 Ā°C tokom 3 sata, ostavljena da se ohladi i sipana je u izmijeÅ”anu vodu (100 ml). RezultirajuÄa smjesa je ekstrahirana sa eterom (2 Ć 150 ml) i kombinirani ekstrakti su isprani sa vodom (50 ml) i ispareni pod sniženim tlakom. Ostatak je proÄiÅ”Äen trituracijom sa heksanom (3 Ć 25 ml), praÄeno kromatografijom stupca na silikagelu (200 g) koristeÄi gradijent elucije heksan:etil acetat (100:0 do 50:50), zatim kristalizacijom iz heksan-diklorometana, radi dobivanja spoja iz naslova kao vrlo blijedo sivi Ävrsti proizvod. A mixture of the title compound of preparation 60 (10.8 g), tri-n-butyl(vinyl)tin (20 ml), tetrakis(triphenylphosphine)palladium(0) (1.0 g) and dimethylformamide (60 ml) was mixed at 75 Ā°C for 3 hours, allowed to cool and poured into mixed water (100 ml). The resulting mixture was extracted with ether (2 x 150 ml) and the combined extracts were washed with water (50 ml) and evaporated under reduced pressure. The residue was purified by trituration with hexane (3 Ć 25 ml), followed by column chromatography on silica gel (200 g) using a gradient elution of hexane:ethyl acetate (100:0 to 50:50), then crystallization from hexane-dichloromethane to give the compound of title as a very pale gray solid product.
Ī“ (CDCl3): 5,46 (d, 1H); 5,92 (d, 1H); 6,63 (dd, 1H); 7,51 (s, 2H); 7,62 (s, 1H). Ī“ (CDCl 3 ): 5.46 (d, 1H); 5.92 (d, 1H); 6.63 (dd, 1H); 7.51 (s, 2H); 7.62 (s, 1H).
MS (termosprej): M/Z [M+NH4] 315,0. MS (thermospray): M/Z [M+NH4] 315.0.
C12H6Cl3N3 + NH4 zahtijeva 315,0. C12H6Cl3N3 + NH4 requires 315.0.
Claims (24)
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Application Number | Priority Date | Filing Date | Title |
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GBGB9625290.3A GB9625290D0 (en) | 1996-12-05 | 1996-12-05 | Parasiticidal agents |
GBGB9702235.4A GB9702235D0 (en) | 1997-02-04 | 1997-02-04 | Parasiticidal agents |
GBGB9712045.5A GB9712045D0 (en) | 1997-06-10 | 1997-06-10 | Parasiticidal agents |
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HRP970663A2 true HRP970663A2 (en) | 1998-10-31 |
HRP970663B1 HRP970663B1 (en) | 2003-10-31 |
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